89 Research jobs

Pharmaceutical Research Associates, Inc. Medical Research Associate 2 - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60519 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117355909

Pharmaceutical Research Associates, Inc. Medical Research Associate - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60823 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117355541

IDC Research Manager, Infrastructure Systems, Platforms and Technologies US-MA-Framingham Job ID: 2019-1590 Type: Regular Full-Time # of Openings: 1 Category: Research IDC Overview IDC is the most respected global technology market research firm operating in over 110 countries worldwide. Our collaborative, innovative and entrepreneurial culture is the perfect place for you to discover your future. IDC's Infrastructure Platforms and Technologies Group is seeking a Research Manager to support its research and business development efforts in this sector. We are looking for an individual that has exposure to or has managed infrastructure technologies, systems and platforms: Current and next-gen infrastructure technologies spanning compute/servers, storage systems and converged infrastructure from leading vendors like Dell, HPE, NetApp, Pure and others. Current and next-gen infrastructure virtualization and orchestration technologies such as VMware vSphere, KVM and Xen, Docker, Kubernetes etc. Converged and hyperconverged infrastructure (e.g. solutions from Dell, VMware and Nutanix), composable/disaggregated infrastructure (e.g. HPE Synergy) and integrated platforms like Exadata. Cloud on-premises solutions from vendors like Amazon Web Services (e.g. AWS Outposts), Microsoft (e.g. AzureStack) and Google (e.g. Anthos) Current and newer storage system architectures, data-persistence and memory technologies Storage and Storage related software solutions including data protection and recovery, copy data management, software-defined storage, archiving and storage device management software. This is a highly visible position that requires the candidate to develop cutting-edge qualitative and quantitative research for IDC's exceptionally diverse base of clients that includes hardware, software and services vendors. Responsibilities Publish and present innovative, insightful, and actionable research: this includes writing well-researched and concise reports, generating forecasts, and presenting findings to vendors. Participate in survey design and analysis: working in cooperation with IDC's primary researchers to develop, execute and publish relevant consumer and enterprise survey data Provide first-class customer support and advisory services: our clients rely on us for timely and actionable insights and ongoing customer interaction is a top responsibility Work closely with other IDC analysts to collect, analyze, and report historical device shipments as well as forecast future shipments Qualifications A broad background that includes understanding of infrastructure hardware and software platforms and technologies, participating vendors and market dynamics. Ability to critically analyze new, disruptive and emerging technologies, products, services and vendors, and express the analysis in a written format. Strong research experience and the ability to develop and maintain quantitative data models for historical and forecast data, develop related qualitative analysis, analyze survey data and deliver documents and projects on a timely basis. Excellent written and oral communications skills. This position requires excellent presentation skills Good social media and blogging skills Ability and ease with working independently and with a team Prior experience working as an analyst and/or related business experience is a plus. A bachelor's degree Experience working with an IT infrastructure vendor is preferred. In addition to the opportunity to join a highly successful and motivated research team, this position offers the successful candidate the opportunity to thrive in the industry's leading provider of market intelligence, delivering expert solutions to major suppliers of cutting-edge infrastructure solutions. About IDC: International Data Corporation (IDC) is the premier global provider of market intelligence, advisory services, and events for the information technology, telecommunications and consumer technology markets. IDC helps IT professionals, business executives, and the investment community make fact-based decisions on technology purchases and business strategy. More than 1,100 IDC analysts provide global, regional, and local expertise on technology and industry opportunities and trends in over 110 countries worldwide. For 50 years, IDC has provided strategic insights to help our clients achieve their key business objectives. IDC is a subsidiary of IDG, the world's leading technology media, research, and events company. IDC is an Equal Opportunity Employer. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, handicap, race, color, religion, gender, gender identity and expression, ancestry, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or other categories protected by law. PI117353014

Oregon Health & Science University Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu. Location: US-OR-Portland Req ID: 2020-3754 Position Category: Faculty/Provider Position Type: Regular Full-Time Job Type: Faculty Department: Emergency Medicine - Center for Health Systems Effectiveness Salary Range: Commensurate with Qualifications Schedule: To be Determined HR Mission: School of Medicine Function/Duties of Position The Research Economist will participate in research and educational activities at the Center for Health Systems Effectiveness (CHSE), an OHSU center devoted to research aimed at improving the value and efficiency of health care. They will develop and collaborate on studies at CHSE related to health economics, reimbursement reform, and Medicaid policy. An important research focus is ongoing Medicaid reform in Oregon, Washington, and other states. This position provides a high level of opportunity to collaborate with individuals from multiple disciplines and to work closely with key policy makers. The Research Economist will also have responsibilities mentoring members of the CHSE research team, collaborating with CHSE research partners, assisting with research project management and participating in center leadership activities. The position may serve as a mentor in quantitative research methods to Emergency Medicine fellows and participate in teaching opportunities within University program related to health economics. Required Qualifications Ph.D. or equivalent doctoral degree in health economics, health services research, health policy, or related fields Demonstrated strong record or promise of publication, interest in or evidence of obtaining extramural funding, and strong potential to sustain a successful research program relevant to the mission of the center Preferred Qualifications Proficiency in statistical programming (R, Stata) Additional Details Apply here online. Please be sure to upload a cover letter and Resume or CV. All are welcome PI117349238

Oregon Health & Science University Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu. Location: US-OR-Portland Req ID: 2020-3759 Position Category: Research Position Type: Temporary Part-Time Job Type: Research Department: Neurology Salary Range: $16.03 - $23.04 Schedule: TBD Hours: 10-14 hours per week HR Mission: School of Medicine Function/Duties of Position The Layton Center is an NIH/NIA-funded Alzheimer's Disease Center, and as such is a recognized leader in national and international efforts to understand and develop treatments for Alzheimer's disease, which conducts studies of innovative and promising treatments, technologies for patient support, genetics, neuroimaging and pathology. We are seeking a temporary Research Assistant 2 position to assist with research coordination and implementation of the SHARP study. This work seeks to maintain or improve African American cognitive health through physical and social activity, and through community education. Responsibilities include community outreach, conducting study visits, data organization and cleaning, coding, and assistance in preparing manuscripts. Required Qualifications Bachelor's degree with major courses in field of research / No experience, OR Associate's degree and 3 years of relevant experience Working knowledge of scientific method and human subjects research Intermediate and experienced knowledge of Word, Excel, and other MS Office programs Detail oriented Self-starter and ability to prioritize work demands and manage time appropriately Ability to speak and communicate clearly, and demonstrate a high level of professionalism Ability to interact patiently and respectfully with elderly volunteers Preferred Qualifications Experience working with older adults and/or community members in a research setting Experience presenting research in community settings Clinical research coordination experience Experience working with senior population All are welcome PI117349093

Oregon Health & Science University Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu. Location: US-OR-Portland Req ID: 2020-3756 Position Category: Research Position Type: Regular Full-Time Job Type: Research Department: Oregon Rural Practice-based Research Network Salary Range: $16.03 per hour Schedule: Monday - Friday Hours: Days HR Mission: School of Medicine Department Overview The Oregon Rural Practice-based Research Network (ORPRN) was established in 2002 at Oregon Health & Science University in Portland. ORPRN is dedicated to improving the health of rural Oregonians through community engaged dialogue, coaching, education and research. ORPRN facilitates a broad variety of clinical health care research, quality improvement projects, and practice transformation efforts in settings serving rural and underserved populations in Oregon. ORPRN is committed to creating a welcoming and inclusive culture. We seek to incorporate diverse perspectives into our work and we value the richness that comes from different points of view. Function/Duties of Position The Research Assistant position will support two projects: Comprehensive Primary Care Plus (CPC+) is a demonstration project to achieve Triple Aim through five comprehensive primary care functions of access, care management, comprehensiveness and coordination, patient engagement and population health. The Community Benefit Initiative Reinvestments (CBIR) Program for the Eastern Oregon Coordinated Care Organization (EOCCO) is a quality improvement program that provides funding and technical assistance to health systems, clinics, public health, social service agencies and community advisory councils, with the goal of improving health care and population health in Eastern Oregon. This position will support both projects through tracking and documenting research team and funded project activities, preparing project reports, and collecting and entering data and information. Responsibilities include: Collect and enter data for projects into databases Track and document activities of the projects for project team and funder reports Prepare project reports Schedule and organize meetings with the research team and stakeholders Support the development of presentations for meetings and conferences Gain familiarity with primary care practices and community stakeholders to support ongoing quality improvement initiatives Required Qualifications Bachelor's Degree / No experience; OR Associate's Degree and 2 years of relevant experience High-level computer knowledge and experience in Microsoft Office Ability to create spreadsheets, data entry forms, queries and reports Experience with PowerPoint presentations Preferred Qualifications 1 - 3 years of experience in research data collection, and tracking data and information Additional Details Apply here online. Please be sure to upload a cover letter and Resume or CV. All are welcome PI117349178

Oregon Health & Science University Oregon Health & Science University values a diverse and culturally competent workforce. We are proud of our commitment to being an equal opportunity, affirmative action organization that does not discriminate against applicants on the basis of any protected class status, including disability status and protected veteran status. Individuals with diverse backgrounds and those who promote diversity and a culture of inclusion are encouraged to apply. To request reasonable accommodation contact the Affirmative Action and Equal Opportunity Department at 503-494-5148 or aaeo@ohsu.edu. Location: US-OR-Portland Req ID: 2020-3815 Position Category: Research Position Type: Regular Full-Time Job Type: Research Department: Oregon Clinical and Translational Research Institute (OCTRI) Salary Range: $38,000 - $46,000 Schedule: Monday - Friday; regular weeknight and rare weekend hours required Hours: 8:30a-5:00p HR Mission: Research Department Overview The Oregon Clinical Translational Research Institute (OCTRI) at OHSU is a catalyst for scientific collaboration, translation of biomedical advances into the community, innovation and research growth in Oregon and beyond. OCTRI's mission is to enhance the efficiency and quality of rigorously translating research ideas into impact. To accomplish our mission, our 80-90 employees spread across 13 teams provide a broad expanse of clinical and translational services that include training, funding, research support, and community engagement. OCTRI is part of the National Center for Translational Sciences (NCATS)-funded CTSA consortium that encompasses 50+ hubs around the country. Visit our website to learn more: octri.org. Function/Duties of Position This position provides instructional support and project coordination for OCTRI's Education and Career Development program, including support for the Human Investigations Program an academic program including a certificate and Masters in Clinical Research. The position assists in the development and delivery of an academic curriculum of courses in the program in collaboration with course directors; and assesses the outcomes of students, trainees and graduates through tracking manuscripts, grants, and persistence in research. Duties and responsibilities include coordinating activities, including scheduling, promotion, and AV setup; assessment, and disseminating educational materials for research education courses; admissions and ongoing support for student and trainee participants; and tracking and evaluating trainee progress and outcomes. Since the academic program serves a unique ‘student' group of clinical and research faculty, fellows and graduates students at OHSU and partner instututions in a variety of departments and research areas, the candidate should have the ability to work with investigators from a wide variety of backgrounds with a problem solving approach and an understanding of their educational objectives in clinical and translational research. Experience in medical research (preferably patient-oriented research) or graduate education and career development is preferred. Candidates must be able to demonstrate a history of self-motivated and detail-oriented work and/or research. Position distinguished by level of both independent and collaborative work with a small team, flexibility to complete multiple tasks and projects through various statges of development and implementation; ability to work effectively under pressure of multiple deadlines. Strong oral and written communication skills and commitment to exceptional customer service is required. Working knowledge of data management is required. Required Qualifications Bachelor's Degree (4 year) with major courses in science, clinical research, or healthcare field; OR AA (2 year) and 3 years of relevant experience Experience in clinical or biomedical research Demonstrated intermediate Microsoft Office Word skills (Tables, graphics, formatting), intermediate Excel skills Familiarity with medical/scientific research terminology in a multidiscplinary setting Working knowledge of data management software and database design Extremely organized self-starter with strong ability to prioritize, set obtainable goals, attention to detail, and commitment to deadlines; work efficiently under pressure of multiple deadlines (able to track multiple tasks and projects through various stages of development and implementation Superior communication (written, verbal and presentation) and interpersonal skills, including ability to communicate clearly, positively and effectively Able to develop detailed project plans, perform project monitoring for appropriate resource utilization, and timelines Able to develop detailed project plans, perform project monitoring for appropriate resource utilization, and timelines Able and willing to learn new technologies and acquire skills as required Superior analytic and quantitative skills Must be sufficiently adaptable to accept and perform, in a timely and effective manner, work assignments that are outside the normal (day-to-day) routine Ability to work in a team environment, as well as ability to work independently Discretionary judgment necessary to handle confidential matters Schedule to be determined by manager and employee. Regular evening and rare weekend hours Work station located in shared office area; frequent interruptions by various staff requesting assistance and information This position requires sitting for at least two hours at a time; heavy use of computers. Able to move freely and quickly between various building/research labs, offices (inside and outside) to collect and/or deliver work Able to lift and carry objects at least 20 pounds; ability to stoop, bend, reach and stretch to access computer hardware, file cabinets and storage units; visual skills and ability to make accurate observations Must be comfortable riding the Portland Aerial Tram Able to perform the essential functions of the position with or without accommodation Preferred Qualifications Advanced degree in public health, biostatistics, or informatics Clinical and translational research experience Experience with research design and data management and analysis Experience with graduate education and curriculum development Knowledge of program evaluation Knowledge of REDCap, Compass, Cognos, Echo 360, website editing tools, Sakai, Oracle, Banner, Audio-Visual (AV) tools Experience with web content creation Experience with grant guidelines and application processes Additional Details Apply here online. To be fully considered for this position, please upload both a cover letter and a resume or CV. All are welcome PI117348418

University of Kentucky Equal Employment Opportunity/M/F/disability/protected veteran status. Posting Details Posting Details Job Title Research Associate Clinical I Requisition Number RE22018 Working Title CRA I (Clinical Phase I) Department Name 7H024:MCC - CLINICAL RESEARCH ORG Work Location Lexington, KY Grade Level 41 Salary Range $14.99-23.98/hour Type of Position Staff Position Time Status Full-Time Required Education BS Click here for more information about equivalencies: http://www.uky.edu/hr/employment/working-uk/equivalencies Required Related Experience 1 yr Required License/Registration/Certification None Physical Requirements Requires handling of light-weight objects up to 10 pounds, sitting for long periods of time, some standing or walking. Shift Monday-Friday 8:00am-4:30pm (40 hrs/wk) Job Summary The primary responsibilities for this position include: obtain, abstract and collate data, reports, etc. related to studies; maintain and submit all reports, forms and updated records to groups required by study; assist in designing a system for organizing, planning and controlling workflow related to the conduct of clinical studies and protocols; coordinate flow of patient through clinical study or protocol, monitoring all events related to patient and communicating any pertinent information to PI and appropriate health professionals. Learn basics of Good Clinical Practice ( GCP) and standard operating procedures ( SOP); monitor safety and general well-being of all patients by exercising independent clinical judgment regarding patient care issues and protocol adherence; assist investigators with identification and recruitment of patients; ensure that per-study and eligibility requirements of the protocol have been met for patients, maintain cooperative and professional relationships with all Clinical Research participants. Collaborate and consult with other health professionals in planning care for study participation and to ensure protocol compliance; and other duties as assigned. Skills / Knowledge / Abilities MS windows, Outlook, Excel, and Word. Does this position have supervisory responsibilities? No Preferred Education/Experience Bachelor's Degree with 2 years experience SoCRA or ACRP certification Deadline to Apply 02/05/2020 University Community of Inclusion The University of Kentucky is committed to a diverse and inclusive workforce by ensuring all our students, faculty, and staff work in an environment of openness and acceptance. We strive to foster a community where people of all backgrounds, identities, and perspectives can feel secure and welcome. We also value the well-being of each of our employees and are dedicated to creating a healthy place to work, learn and live. In the interest of maintaining a safe and healthy environment for our students, employees, patients and visitors the University of Kentucky is a Tobacco & Drug Free campus. As an Equal Opportunity Employer, we strongly encourage veterans, individuals with disabilities, women, and all minorities to consider our employment opportunities. Any candidate offered a position may be required to pass pre-employment screenings as mandated by University of Kentucky Human Resources. These screenings may include a national background check and/or drug screen. Posting Specific Questions Required fields are indicated with an asterisk (*). * University of Kentucky HealthCare seeks to attract, develop and retain highly skilled and competent employees, to provide the best experience for every patient, every time. If selected for a position, do you agree to abide by the UK HealthCare Values of diversity, innovation, respect, compassion, and teamwork? Yes No * University of Kentucky HealthCare recognizes a set of values that guide us in our daily interactions. By applying for a position within UK Healthcare, you are indicating your commitment and expressing your agreement to our five values. These values are diversity, innovation, respect, compassion, and teamwork. Please choose one of the UK Healthcare values and give a specific example when you exhibited this quality in your professional experience. (Open Ended Question) * Please choose the answer that best describes your amount of paid, full-time experience working with IRBs, protocol submissions, and patient consents. None More than 0, up through 1 year More than 1 year, up through 2 years More than 2 years, up through 3 years More than 3 years * Please select the response that best represents your amount of paid, full-time employment experience working with clinical research studies and/or administering or monitoring research protocols. None More than 0, up through 1 year More than 1 year, up through 2 years More than 2 years, up through 3 years More than 3 years * Please describe your experience working with clinical research, data management, study coordination, patient care, and/or patient recruitment and enrollment. (Open Ended Question) * Where did you first see this position advertised other than on UK's online employment system? InsideHigherEd.com HigherEdJobs.com Diverseeducation.com (Diverse Issues in Higher Education) HERCjobs.org (Higher Education Recruitment Consortium) InsightIntoDiversity.com Latinosinhighered.com HospitalCareers.com Indeed.com LinkedIn.com Institute for Diversity in Health Management A Colleague, Friend and/or Family Member None of the Above Applicant Documents Required Documents Resume Cover Letter Optional Documents PI117344168

IDC Senior Research Analyst, Worldwide Enterprise Trackers US-MA-Framingham Job ID: 2019-1545 Type: Regular Full-Time # of Openings: 1 Category: Tracker IDC Overview IDC’s Worldwide Enterprise Infrastructure Tracker group is looking for an individual with superior analytical, communication and data management skills to be part of our team tracking the global enterprise hardware marketplace (datacenter infrastructure and related technologies, e.g. cloud and workloads), and managing the ongoing coordination between a wide range of regional analyst teams across the globe. Upon joining IDC, you can expect a fast-paced and fulfilling work environment along with a culture that rewards and recognizes achievement. We are the most respected global technology market research firm operating in over 110 countries worldwide. Our collaborative, entrepreneurial and innovative culture is the perfect place for you to discover your future. Responsibilities Operations related to IDC’s quarterly Trackers research – including set up of internal tools, coordinating research deadlines, developing and enforcing data quality checks, product delivery, and business development product updates. Continuous testing, evaluation and improvement of internal tools for IDC's global Tracker products Project management and coordination of semiannual end-user survey research Provide timely and accurate support for client inquiries Support IDC sales executives to seek business development opportunities Qualifications Undergraduate degree – preferably in Mathematics, Statistics or Economics 4+ years of market research, survey development or data analyst experience in the IT industry Advanced use of Microsoft Excel (Access or SQL is a plus) Experience in quality control, data analysis, data mining, and project management A well-rounded understanding of the datacenter infrastructure technologies, market dynamics, market players, and market trends Aptitude to work under pressure and coordinate the important work of team members across the globe to meet intense deliverable schedule. Ability to work independently with guidance and in a virtual team environment 1-2 plus years of experience in Project Management managing multiple projects with minimal supervision; managing all phases of the project life cycle, including running project status meetings Ability to collaborate with a technical and service-oriented team of professionals, and promote cooperation from a wide variety of stakeholders, including team members and other internal departments Some travel may be required The position does not have additional budget for sponsorship. About IDC: International Data Corporation (IDC) is the premier global provider of market intelligence, advisory services, and events for the information technology, telecommunications and consumer technology markets. IDC helps IT professionals, business executives, and the investment community make fact-based decisions on technology purchases and business strategy. More than 1,100 IDC analysts provide global, regional, and local expertise on technology and industry opportunities and trends in over 110 countries worldwide. For 50 years, IDC has provided strategic insights to help our clients achieve their key business objectives. IDC is a subsidiary of IDG, the world's leading technology media, research, and events company. IDC is an Equal Opportunity Employer. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, handicap, race, color, religion, gender, gender identity and expression, ancestry, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or other categories protected by law. PI117323222

Morrison & Foerster LLP ID: 7490 Job Posting Title: Research Analyst: Corporate Location: New York Morrison & Foerster LLP, an Am Law 50 law firm with 17 offices worldwide, has an opening for a Research Analyst within our Research Services Department in our New York office. The Opportunity Join the Research Services team of a billion dollar global law firm in a dynamic fast-paced Research Analyst role. The Research Analyst works as part of a firmwide team to provide research expertise for business development efforts and client work. This individual monitors and identifies information sources and data to identify potential opportunities and presents research findings clearly and concisely. The Analyst also participates on firmwide project teams. As part of the firmwide research team, provide research expertise to support the firm's practice areas and business development efforts, including research related to markets, industries, and competitors. Retrieve, package, and present information in response to requests from attorneys and colleagues in research function as well as other departments in the Firm. Handle a high volume of routine research requests including document retrieval requests, requests to mine websites and other sources, and requests to populate spreadsheets with specified data. Create current awareness tools, newsletters, and alerts for ongoing monitoring of clients, industries, and events. Demonstrate strong writing skills and the ability to distill and present research work product in a concise, professional manner. Ideal Candidate Strong background in research focusing on a variety of corporate practices and transactions preferred. Bachelor's degree required plus a minimum of two years related experience or equivalent combination of relevant education and experience. Master's degree in Library Science or Information Science or equivalent degree such as a J.D., M.B.A., or other advanced degree is a plus. Knowledge of the legal materials and databases used to support the Firm's practice areas and research needs for client work and for business development efforts. Demonstrate strong research skills and a deep understanding of research strategies. Who We Are At Morrison & Foerster, our culture is defined by our deeds. We're passionate about what we do. We're equally passionate about how we do it. We resist hierarchies and operate within a model of respect - for our colleagues, their ideas, and the differences that make us stronger. We encourage you to learn more about who we are , and what we do . Should you find you're ready to do the best work of your life, we encourage you to let us know! Morrison & Foerster is an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, sex, religion, creed, ethnic or national origin, ancestry, age, disability, veteran or military status, marital status, pregnancy, sexual orientation, gender identity, domestic partner status, and other categories protected by applicable laws, or in retaliation for opposition to any practices forbidden under this policy. PI117309969

Are you compassionate? Do you love animals? The Animal Care Technician provides basic husbandry services or perform tasks involved in the care, maintenance, and welfare of animals (e.g. mice, rats, rabbits, swine, canines, non-human primates). DP-IND Responsibilities Comply with the appropriate safety and study requirements as described in the Standard Operating Procedures (SOPs), Good Laboratory Practices (GLP) and governmental regulations. Comply with appropriate safety and health practices including personal protective equipment and barrier requirements, as applicable. Perform animal identification tasks (tattoo, sex, ear tag, etc.). Recognize animal behavior, health status and report to appropriate channels. Perform animal husbandry (clean, feed, sanitation, enrichment, etc.) on a regular basis. Operate, maintain, and perform equipment tasks (e.g. cage washers, autoclave, cage movement, etc.) on a regular basis. Observe and report any aberrations in animal room environments (room temperature, humidity, lighting, ventilation, vermin, etc.). Perform general facility cleaning, stocking, and inventory. Prepare rooms, sanitize, and repair as needed. Receive, and distribute animals for isolation, study assignment or consolidation. Attend training programs to become more knowledgeable of and develop expertise in laboratory animal science. What We Offer: Competitive salary Medical/Dental/Vision insurance 401K Life insurance Relaxed dress code Paid holidays Paid Time Off On-site cafeteria and gym Company events, including happy hours, team building competitions, lunches and much more. Qualifications A diploma from high school or equivalent is required. This is an entry level position and previous animal experience would be beneficial. AALAS certification preferred. Basic computer and math skills. Ability to effectively comprehend and communicate (verbal and written) in a professional manner. An aptitude to follow company policies (tobacco, drug and alcohol-free site), standard operating procedures, and maintain regulatory compliance is important. This is a physical position in a warm environment. Position requires the ability to bend, squat, kneel, and stand, for up to 7 hours/day. Be able to regularly push and pull heavy objects and safely move or lift heavy loads (up to 50 pounds). Ability to work collaboratively with all levels of employees. Ability to multi-task and maintain organization in a fast paced, changing environment. Positive attitude toward work and co-workers. Be a part of a team that likes to work hard and have fun. All schedules include weekends, holidays and occasional overtime. PI117310879

IDC Human Resources Business Partner US-MA-Framingham Job ID: 2019-1613 Type: Regular Full-Time # of Openings: 1 Category: Human Resources IDC Overview IDC is the most respected global technology market research firm operating in over 110 countries worldwide. Our collaborative, innovative and entrepreneurial culture is the perfect place for you to discover your future. The IDC Human Resources team is seeking a confident and strategic Human Resources Business Partner to partner and consult with senior leaders across the Research and Product Management and Marketing teams in such areas as recruitment, compensation planning, employee relations, performance management and organizational design and development. This position is a full-time role located at IDC headquarters in Framingham MA. Responsibilities The HR Business Partner will report to the CHRO and will direct all aspects of HR initiatives for their client base. They will build internal business partnerships, provide developmental coaching to all levels of the organization and offer creative solutions to business issues. They will learn the research business and understand the goals and challenges in order to translate business objectives into the appropriate HR actions and initiatives including: Independently recruit for open positions in their client base, including strategic sourcing and hiring of top talent Managing and facilitate resolution of employee relation matters Coach managers through performance management process and performance improvement plans Consult on C ompensation Planning Manage reorganizations and organizational development Collaborate with other HR team members on HR related programs and practices Act as an agent for change Qualifications This position requires a Bachelor’s D egree and a minimum of 6-10 years of proven HR generalist experience. Knowledge of technology/consulting services, market research related environments is a plus. The ideal candidate must be able to work independently, be detail oriented and able to interact with employees across all levels of the organization. Recruiting experience and the ability to develop creative solutions and facilitat e resolutions in a fast-paced environment is required. Must be a team player and possess a great sense of humor and collaborative attitude Excellent organizational, written and verbal communication skills and attention to detail is required. Experience as a trusted partner to senior leaders is desired. Must have strong building relationship skills and ability to travel from time to time. Must be technically proficiency with Office 365 and have experience using an ATS and associated HR databases. Ultimate software and iCIMS experience is a bonus. About IDC: International Data Corporation (IDC) is the premier global provider of market intelligence, advisory services, and events for the information technology, telecommunications and consumer technology markets. IDC helps IT professionals, business executives, and the investment community make fact-based decisions on technology purchases and business strategy. More than 1,100 IDC analysts provide global, regional, and local expertise on technology and industry opportunities and trends in over 110 countries worldwide. For 50 years, IDC has provided strategic insights to help our clients achieve their key business objectives. IDC is a subsidiary of IDG, the world's leading technology media, research, and events company. IDC is an Equal Opportunity Employer. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, handicap, race, color, religion, gender, gender identity and expression, ancestry, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or other categories protected by law. PI117279868

IDC Research Manager Digital Experience Management Software US-MA-Framingham Job ID: 2019-1592 Type: Regular Full-Time # of Openings: 1 Category: Research IDC Overview IDC is seeking an experienced software research analyst to join its Content Management market research and advisory group. The Research Manager will be responsible for developing research across several content-centric software technologies including digital experience management ( web content management , digital asset management , product information and content management , content sourcing/curation and content marketing platforms , video platforms ) and/or the enterprise content ecosystem, including ECM, content sharing and collaboration, document automation, and related domains . Important research topics include the role of AI and other innovation accelerators in in the content lifecycle and supply chain and the opportunity to rearchitect content centric workflows for content agility The Research Manager will also participate in key IDC initiatives including the Future of Work, Future of Intelligence and Future of Customer. Responsibilities The ideal candidate will be innovative and resourceful, with a good mix of technical, analytical, writing and communication capabilities. The role includes client-facing and industry-facing responsibilities, as well as responsibility for producing thought-provoking, deep, and actionable market analysis via a broad range of research deliverables (e.g. white papers, surveys, infographics, blogs, presentations, etc.) products in the areas of content technologies and related domains. The Research Manager will also be involved with consulting, advisory services and custom research deliverables. The ideal candidates will possess four primary skill sets: Excellent interpersonal skills for supporting both client inquiry and internal collaboration with other IDC analysts, including the ability to collaborate in a global environment Strong analytical and quantitative and modeling skills Excellent written and verbal communication and presentation skills Solid business development and client relationship capabilities Related experience in one or more of the relevant domains: digital experience management, web content management, digital asset management, product information and content management, content sourcing/curation and content marketing platforms, video platforms, enterprise content management, content sharing and collaboration and document automation. Qualifications Bachelor's degree required, MBA a plus 5-10 years of previous market research or related industry experience Strong, demonstrated written communication skills, including writing of reports, presentations, or other documents that are actionable and relevant for the target audience Strong, demonstrated verbal (including public speaking) skills Proficiency in Microsoft suite of products is a must. Advanced skills in Excel required; knowledge of analytic tools for social sciences market research preferred Ability to travel (<25%) will be required on an as needed basis Demonstrated ability in working under pressure with competing deadlines Sound judgment, planning, project management and organization skills Ability to analyze quantitative and qualitative data to derive trends and research agendas IDC is an Equal Opportunity Employer. Applicants and employees are considered for positions and are evaluated without regard to mental or physical disability, handicap, race, color, religion, gender, gender identity and expression, ancestry, national origin, age, genetic information, military or veteran status, sexual orientation, marital status or other categories protected by law. PI117279924

Pharmaceutical Research Associates, Inc. Medical Research Associate PRN - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60712 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117266624

Pharmaceutical Research Associates, Inc. Medical Research Associate PRN - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60711 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117266639

Pharmaceutical Research Associates, Inc. Medical Research Associate PRN - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60710 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117266654

Pharmaceutical Research Associates, Inc. Medical Research Associate PRN - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60708 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117266669

Pharmaceutical Research Associates, Inc. Medical Research Associate PRN - Salt Lake City US-UT-Salt Lake City Job ID: 2020-60707 Type: US-Southwest # of Openings: 1 Category: Clinical Trial Support PRA Health Sciences Overview Do you want to watch clinical development change, or do you want to be the one to shape it? Because we’re hoping you’re here for the latter. Who are we? We Are PRA. We are 16,000 employees strong, operating in more than 85 countries. We are committed to saving lives and we are constantly striving to be the best at what we do. Our impact is real and we see it every single day. We help get life-saving drugs into the hands of those who need them most. Who are you? Are you a recent Medical Assistant Grad looking for experience? Or maybe a skilled CNA, EMT, or Phlebotomist, looking to use your skills in an ever-changing environment? Or, a healthcare professional looking for a career that can impact the lives of millions? Still with me? Good! Then an opportunity as a Medical Research Associate in our Clinical Research Organization is the career for you! Responsibilities What will you be doing? In short, you will be responsible for meeting/greeting clinical research volunteers as they come into the clinic, checking their vitals (height, weight, blood pressure, BMI), and essentially making sure the study participants are healthy enough to participate in the clinical trial according the protocol of a study. Clinict Tasks: Screen potential subjects. Performs basic medical procedures according to protocol for specified study participants, including but not limited to informed consent, vital signs, Height,/Weight/BMI measurements, meals, water fast, phlebotomy (straight stick/draw from IV catheters), finger stick blood sugar, ECGs, UA, UDS, urine collection, fecal collection, pulse oximetry, AE/ConMed assessment , obtain medical history and assists with Investigational Product accountability Ensures all study activities/procedures (during screening and clinical procedures) are completed on schedule and in accordance with the protocol, the FDA and the IRB requirements. Performs non-medical activities such as distribution of scrubs, locks, DVDs, movies, games, front desk tasks (screening centre) etc. Monitors subject safety. Reports equipment malfunctions and may assist with specified equipment maintenance and stocking of supplies. Performs general housekeeping duties as needed, including cleaning and making dorm beds, wiping down bedside tables, organizing subject resting and entertainment areas, cleaning screening exam rooms, etc. Communication/Training/Meetings: Assist with study setup activities and perform check-in and check-out activities. (Interacts with clients when appropriate (following proper communication path if needed) and ) perform/collect volunteer surveys Complete training activities required for Level I. Learn mentor/training activities with assigned mentor if applicable. Attend staff meetings, briefings, etc Explain and enforce / maintain subject house rules Warn appropriate staff in case of medical emergency Data Collection/Queries : Accurately documents all study procedures on CRF/SDs. Resolve data queries within 24hr period Qualifications What do you need to have? Read, write, and speak English; fluent in host country language required. High School Diploma or G.E.D. required. Undergraduate degree in a clinical, health- related area and/or minimum 1 year of equivalent work experience with similar position 1+ years work experience in a medical or clinical field preferred Basic Life Support (BLS)/Phlebotomist Certification preferred Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, or Laboratory Technician preferred. To qualify, applicants must be legally authorized to work in the United States, and should not require, now or in the future, sponsorship for employment visa status. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans, and individuals with disabilities PI117266684