1020 clinical research coordinator jobs found

The Clinical Research Coordinator (CRC) coordinates, implements and completes clinical research studies and/or clinical trials in the Urology and Surgery Departments by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned Understands and can conduct clinical research studies that require but not limited...

Clinical Research Coordinator I Med-Anesthesiology and Perioperative Medicine - Pennsylvania-Pittsburgh - (25006206) Job Summary Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Recruits research subjects and conducts interviews and research assessments. Essential Functions Assists with and adheres to Institutional Review Board (IRB) renewal, modification, and approved protocols. Recruits research subjects and conducts interviews and research assessments. Physical Effort Must be able to sit for prolonged periods of time. Assignment Category: Full-time regular Job Classification: Staff.Clinical Research Coordinator I Job Family: Research Job Sub Family: Clinical Research Campus: Pittsburgh Minimum Education Level Required: Bachelor's Degree Minimum Years of Experience Required: No experience required Will this position accept substitution in...

Job Ref:46567 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Clinical Research Coordinator will work closely with Lachelle D. Weeks MD, PhD, an investigator in the Division of Population Sciences and Director of the CHIP Clinic in the Center for Early Detection and Interception of Blood Cancers. Dr. Weeks’s research focuses on identifying patients at risk for developing the blood cancers myelodysplastic syndrome and acute myeloid leukemia (MDS/AML). She led the development of the first clinically validated risk model for clonal hematopoiesis (CH), a preleukemic condition that is common in older adults. The clonal hematopoiesis risk score (CHRS) estimates a patient’s risk of progressing from CH to MDS/AML and is now used in clinics at DFCI and around the world. Dr. Weeks also investigates the relationship between CH and non-cancer outcomes, such as autoimmune...

Job Ref:46496 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Clinical Research Coordinator (CRC) will work within the Center of Cancer Therapeutic Innovation (CCTI) department supporting the clinical research program and research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen...

Job Ref:45929 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Clinical Research Coordinator work within the Breast Oncology clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain informed consent,...

Job Ref:46089 Location:1 Patriots Place, Foxborough, MA 02035 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Clinical Research Coordinator work within the Dana-Farber Regional Campus clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator(s) and the DFCI disease programs. The Regional Campus CRC will be responsible for the primary data collection, management of patient clinical information, and regulatory documents as it pertains to participation in clinical trials across all studies open at the Regional Campus site(s).  Ensures timely collection of protocol related samples including shipment to outside entities as required.  Maintains site regulatory binders and ensures study compliance with all state, federal, and IRB requirements.  May be responsible for site IRB submissions...

Job Ref:46866 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Clinical Research Coordinator work within the Genitourinary Oncology (GU) clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures timely collection of protocol related samples including shipment to outside entities as required. Maintains regulatory binders and ensures study compliance with all state, federal, and IRB requirements. May be responsible for IRB protocol submissions (amendments, continuing reviews, and minimal risk protocols). This individual may also screen patients for protocol eligibility, obtain...

Job Ref:46707 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 4-5 days onsite/week Overview The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking a Clinical Research Coordinator (CRC) to join the clinical research team. The GI Oncology Clinical Research Program supports PI initiated, industry sponsored, and cooperative group phase I - IV clinical trials across multiple GI cancers, including esophageal, stomach, liver, pancreas, colon, and neuroendocrine.The Clinical Research Coordinator work within the clinical research program and support the research team in the overall conduct of clinical trials using Good Clinical Practice under the auspices of the Principal Investigator. The CRC will be responsible for the primary data collection and management of patient clinical information as it pertains to participation in clinical trials. Ensures...

Clinical Research Coordinator in Emergency Department - Coordinates, implements and completes clinical research studies and/or clinical trials by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned. Understands and can conduct clinical research studies that require but not limited to Emergent...

The Clinical Research Coordinator coordinates, implements and completes clinical research studies and/or clinical trials in the Neonatology Department at the Nemours Philadelphia Thomas Jefferson University location by assisting in regulatory document preparation and collection, in-servicing research teams, recruiting study participants, obtaining parental permission/assent/consent forms, educating parents/participants, scheduling and conducting study procedures, collecting and recording study data, maintaining detailed study records, interfacing with study sponsors, participation in sponsor study monitoring visits, prepare for and participate in internal and external research audits, maintain various research databases. Essential Functions Follows all aspects of Standard Operating Procedures and Good Clinical Practices in the conduct of clinical research; collects and prepares documents as required by sponsoring agencies; attends Investigator Meetings, as assigned Understands...

University of Kentucky Equal Employment Opportunity/M/F/disability/protected veteran status. Posting Details Posting Details Job Title STEPS Clinical Research Coordinator I Requisition Number TE09115 Department Name 7H853:NEUROSURGERY Work Location Lexington, KY Salary Range $30.00/hour Type of Position Temporary Position Time Status Part-Time Required Education Required Related Experience Required License/Registration/Certification Physical Requirements Sitting for extended periods of time, walking, lifting/pushing objects up to 50 lbs Shift Work Shift: 8am-4:30pm Job Summary This position is responsible for managing study protocols and ensuring compliance with regulatory requirements. The role involves collaboration with Principal Investigators and research team members to support all aspects of study planning, execution, and oversight. Duties include preparing and submitting IRB...

Job Ref:46665 Location:450 Brookline Ave, Boston, MA 02215 Category:Clinical Research Employment Type:Full time Work Location:Onsite: 100% onsite Overview Dana-Farber’s Division of Population Sciences is seeking a Clinical Research Coordinator II to support a multidisciplinary, multi-center implementation project designed to improve participation of underrepresented patients in blood cancer research across the Dana-Farber network. Building on extensive institutional efforts to expand access to clinical trials, this role will coordinate complementary research interventions; manage day-to-day study operations; and collaborate closely with research navigators, clinicians, scientists, patients, and administrative stakeholders, including OnCore Data Informatics team and Office for Human Research Studies (OHRS). The CRC II will report directly to the Principal Investigator and contribute to aligned research evaluating barriers in the delivery of cancer research...

Job Title: Clinical Research Coordinator - Grant Funded - Department of Medicine Clinical Research Unit Description Employment Status: Full time Shift: Variable Hours (United States of America) Facility: 213 S Jefferson St - Roanoke CP01 Carilion Medical Center. Requisition Number: R151805 Clinical Research Coordinator - Grant Funded - Department of Medicine Clinical Research Unit (Open) How You’ll Help Transform Healthcare: Under general supervision of the Principal Investigator, the Clinical Research Coordinator I assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy. Under general supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or...

The Clinical Research Coordinator I is responsible for coordinating and performing research related activities for clinical research projects as assigned. The primary purpose of this position is to oversee the screening, enrollment, and retention of study participants, ensuring quality data collected throughout the research study, and implementing the procedures and activities under the direction and oversight of the lead coordinators and principal investigators of the projects. Minimum Qualifications: \n Bachelor's degree in a related field -OR- equivalent combination of education and experience. \n Preferred Qualifications: \n Strong working knowledge in Microsoft Office programs and other software packages. Medical and research terminology, processes and procedures, phlebotomy experience, ECG training. \n Working at USF \n With approximately 16,000 employees, the University of South Florida is one of the largest employers in the Tampa Bay area. We are dedicated to...

SUMMARY The Clinical Research Coordinator (CRC) is responsible for the coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The CRC will work collaboratively with the principal investigator (PI), the Sr. Clinical Research Coordinator (SCRC), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The CRC will assist the PI in protecting the rights, safety and welfare of all study participants. Essential Duties and...

SUMMARY The Senior Clinical Research Coordinator (SCRC) is responsible for the facilitation and coordination of daily clinical trial activities. USRC has a research Partnership with the principal investigator (PI) and their physician practice. The local oversight and direction for activities related to the conduct of the clinical research is directed by the PI. The SCRC will work collaboratively with the principal investigator (PI), the clinical site, sponsor(s), clinical research organization(s) (CROs), institutional review boards (IRBs), and study participants to ensure Execution of the clinical trial in accordance with the Study Protocol, the Food and Drug Administration (FDA), International Council for Harmonization of Technical Requirements for Pharmaceuticals for Human Use (ICH) and applicable state and local regulations. The SCRC will assist the PI in protecting the rights, safety and welfare of all study participants. Essential Duties and Responsibilities include the...

Job Title: Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator Description Employment Status: Full time Shift: Variable Hours (United States of America) Facility: 213 S Jefferson St - Roanoke CP01 Carilion Medical Center. Requisition Number: R155535 Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator (Open) How You’ll Help Transform Healthcare: Make the most of your clinical skills at an organization that has earned numerous awards for clinical excellence. Based in Roanoke, VA, our community-based health care organization encompasses a comprehensive network of hospitals, primary and specialty physician practices, and other complementary services. The Clinical Research Coordinator manages administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by...

Job Title: Clinical Research Coordinator - Department of Medicine Clinical Research Unit - Grant Funded Description Employment Status: Full time Shift: Variable Hours (United States of America) Facility: 213 S Jefferson St - Roanoke CP01 Carilion Medical Center. Requisition Number: R154601 Clinical Research Coordinator - Department of Medicine Clinical Research Unit - Grant Funded (Open) How You’ll Help Transform Healthcare: Under minimal supervision of the Principal Investigator, the Clinical Research Coordinator II assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or internally funded studies while maintaining compliance with guidelines set by governing agencies and institutional policy. Under minimal supervision of the Principal Investigator, assists with administrative activities associated with the conduct of research studies including industry sponsored, grant funded or...

Clinical Research Coordinator, Senior US-OR-Portland Requisition ID: 2025-36498 Position Category: Research Job Type: Research Position Type: Regular Full-Time Posting Department: Neurology Posting Salary Range: $24.10 - $36.14 per hour Posting FTE: 1.00 Posting Schedule: M-F Posting Hours: 8:00am - 4:30pm HR Mission: School of Medicine Drug Testable: Yes Function/Duties of Position The Division of Movement Disorders has an opening for a TI Senior Clinical Research Assistant (Clinical Research Coordinator, Sr).  The Clinical Research Coordinator is a highly organized and motivated individual responsible for coordinating multiple complex therapeutic interventional trials related to Parkinson's Disease and Movement Disorders.  The senior coordinator will perform study procedures per the research study protocols and regulatory requirements, with minimal supervision, while adhering to study protocol timelines and working closely with the Principal...

The Clinical Research Coordinator I is responsible for coordinating and performing research related activities for clinical research projects as assigned. The primary purpose of this position is to oversee the screening, enrollment, and retention of study participants, ensuring quality data collected throughout the research study, and implementing the procedures and activities under the direction and oversight of the lead coordinators and principal investigators of the projects. \n This Position is 100% Grant-Funded. \n This Position is not eligible for Visa Sponsorship. \n• Bachelor's degree in a related field -OR- equivalent combination of education and experience. Working at USF \n With approximately 16,000 employees, the University of South Florida is one of the largest employers in the Tampa Bay area. We are dedicated to cultivating a talented, engaged and driven workforce that strives to be bold. Employees excel in USF's rich academic environment, which fosters their...