Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Safety Data Coordinator 2 US-KS-Lenexa Job ID: 2020-60500 Type: US-Midwest # of Openings: 1 Category: Drug Safety PRA Health Sciences Overview Leads the development and implementation of medical coding in clinical data management systems; participates in management of individual case safety reports (SAEs, AEs of Special Interest, Adverse Drug Reactions), AE/SAE reconciliation and data retrievals from the clinical and/or safety databases; provides support for endpoint adjudication committees. Responsibilities Performs consistent coding of adverse events, medical history, concomitant medications and other terms according to the project-specific coding conventions. Reconciles SAE/AE between clinical and safety database in accordance with the SAE/AE reconciliation plan and other project-specific guidelines. Generates DCFs (Data Clarification Forms) or queries, performs corrections of CRFs, if applicable, and clinical databases in accordance with DCF replies. Receives and tracks serious adverse events, adverse events of special interest, and adverse drug reactions reports and forwards them to the sponsor/third party in accordance with project-specific contractual agreement. Performs data entry of minimal SAE/ADR data in company’s or sponsor's safety database. Queries site or reporter for inconsistent or incomplete information on SAE/ADR report. Maintains address lists for submission of safety reports to investigators and EC/IRBs. Tracks submission of safety reports to investigators and EC/IRBs in company’s Safety Letter Tracking System. Conducts quality review of endpoint dossiers/adjudication forms adhering to the agreed timelines. Tracks and reconciles endpoint dossiers/adjudication forms. Queries sites for missing or inconsistent information on endpoint dossiers/adjudication forms. Interacts with endpoint committee during endpoint review. Properly documents all internal and external contacts and communications. Consistently meets or exceeds objectives set annually. Ensures personal career goals are set each year and progress is monitored for completion Performs consistent coding of adverse events, medical history, concomitant medications and other terms according to the project-specific coding conventions. Reconciles SAE/AE between clinical and safety database in accordance with the SAE/AE reconciliation plan and other project-specific guidelines. Generates DCFs (Data Clarification Forms) or queries, performs corrections of CRFs, if applicable, and clinical databases in accordance with DCF replies. Receives and tracks serious adverse events, adverse events of special interest, and adverse drug reactions reports and forwards them to the sponsor/third party in accordance with project-specific contractual agreement. Performs data entry of minimal SAE/ADR data in company’s or sponsor's safety database. Queries site or reporter for inconsistent or incomplete information on SAE/ADR report. Maintains address lists for submission of safety reports to investigators and EC/IRBs. Tracks submission of safety reports to investigators and EC/IRBs in company’s Safety Letter Tracking System. Conducts quality review of endpoint dossiers/adjudication forms adhering to the agreed timelines. Tracks and reconciles endpoint dossiers/adjudication forms. Queries sites for missing or inconsistent information on endpoint dossiers/adjudication forms. Interacts with endpoint committee during endpoint review. Properly documents all internal and external contacts and communications.Consistently meets or exceeds objectives set annually. Ensures personal career goals are set each year and progress is monitored for completion. Responsible for effective and efficient development of the coding conventions and coding dictionary license confirmation forms. Manages quality control review of coded data. Responsible for effective and efficient development of the SAE/AE reconciliation plan. Performs quality control of minimal data entry of safety data into company’s or sponsor's safety database. Assures consistency of plans with client contract and identifies out of scope activities promptly and accurately. Participates in internal and client meetings. Reports project status to project/functional management. Adheres to financial and administrative processes, such as managing project budget and timelines, estimation of resource needs and projected hours. Qualifications Undergraduate degree or its international equivalent, preferably in life science and/or healthcare professional. Read, write and speak English; fluent in host country language required. Previous experience using computerized information systems and standard application software (Windows, MS Office). Good written and oral communication skills. 3 Years Data Management or Health information Management experience required PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224439
Jan 18, 2020
Pharmaceutical Research Associates, Inc. Safety Data Coordinator 2 US-KS-Lenexa Job ID: 2020-60500 Type: US-Midwest # of Openings: 1 Category: Drug Safety PRA Health Sciences Overview Leads the development and implementation of medical coding in clinical data management systems; participates in management of individual case safety reports (SAEs, AEs of Special Interest, Adverse Drug Reactions), AE/SAE reconciliation and data retrievals from the clinical and/or safety databases; provides support for endpoint adjudication committees. Responsibilities Performs consistent coding of adverse events, medical history, concomitant medications and other terms according to the project-specific coding conventions. Reconciles SAE/AE between clinical and safety database in accordance with the SAE/AE reconciliation plan and other project-specific guidelines. Generates DCFs (Data Clarification Forms) or queries, performs corrections of CRFs, if applicable, and clinical databases in accordance with DCF replies. Receives and tracks serious adverse events, adverse events of special interest, and adverse drug reactions reports and forwards them to the sponsor/third party in accordance with project-specific contractual agreement. Performs data entry of minimal SAE/ADR data in company’s or sponsor's safety database. Queries site or reporter for inconsistent or incomplete information on SAE/ADR report. Maintains address lists for submission of safety reports to investigators and EC/IRBs. Tracks submission of safety reports to investigators and EC/IRBs in company’s Safety Letter Tracking System. Conducts quality review of endpoint dossiers/adjudication forms adhering to the agreed timelines. Tracks and reconciles endpoint dossiers/adjudication forms. Queries sites for missing or inconsistent information on endpoint dossiers/adjudication forms. Interacts with endpoint committee during endpoint review. Properly documents all internal and external contacts and communications. Consistently meets or exceeds objectives set annually. Ensures personal career goals are set each year and progress is monitored for completion Performs consistent coding of adverse events, medical history, concomitant medications and other terms according to the project-specific coding conventions. Reconciles SAE/AE between clinical and safety database in accordance with the SAE/AE reconciliation plan and other project-specific guidelines. Generates DCFs (Data Clarification Forms) or queries, performs corrections of CRFs, if applicable, and clinical databases in accordance with DCF replies. Receives and tracks serious adverse events, adverse events of special interest, and adverse drug reactions reports and forwards them to the sponsor/third party in accordance with project-specific contractual agreement. Performs data entry of minimal SAE/ADR data in company’s or sponsor's safety database. Queries site or reporter for inconsistent or incomplete information on SAE/ADR report. Maintains address lists for submission of safety reports to investigators and EC/IRBs. Tracks submission of safety reports to investigators and EC/IRBs in company’s Safety Letter Tracking System. Conducts quality review of endpoint dossiers/adjudication forms adhering to the agreed timelines. Tracks and reconciles endpoint dossiers/adjudication forms. Queries sites for missing or inconsistent information on endpoint dossiers/adjudication forms. Interacts with endpoint committee during endpoint review. Properly documents all internal and external contacts and communications.Consistently meets or exceeds objectives set annually. Ensures personal career goals are set each year and progress is monitored for completion. Responsible for effective and efficient development of the coding conventions and coding dictionary license confirmation forms. Manages quality control review of coded data. Responsible for effective and efficient development of the SAE/AE reconciliation plan. Performs quality control of minimal data entry of safety data into company’s or sponsor's safety database. Assures consistency of plans with client contract and identifies out of scope activities promptly and accurately. Participates in internal and client meetings. Reports project status to project/functional management. Adheres to financial and administrative processes, such as managing project budget and timelines, estimation of resource needs and projected hours. Qualifications Undergraduate degree or its international equivalent, preferably in life science and/or healthcare professional. Read, write and speak English; fluent in host country language required. Previous experience using computerized information systems and standard application software (Windows, MS Office). Good written and oral communication skills. 3 Years Data Management or Health information Management experience required PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224439
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Lab Sample Receipt Associate - Lenexa, KS US-KS-Lenexa Job ID: 2020-60684 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities Sample Management: Receives, inventories, monitors, documents and stores samples according to appropriate storage conditions. Performs data entry into Watson and other appropriate tracking spreadsheets to account for all specimens received. Informs Project Manager (PM) and Bioanalytical Team Leader (BTL) of sample receipt. Destroys samples and creates appropriate documentation of sample destruction after approval of the PM. Ordering of general laboratory supplies: Orders and tracks general laboratory supplies. Checks receipts of general laboratory supplies and report defects. Processes and register of general laboratory supplies. General Laboratory Support: Coordinates disposal of waste materials. Periodically registers temperatures of freezers and refrigerators. Project Management Support: Inform Project Manager (PM) and Bioanalytical Team Leader (BTL) on receipt of samples. Reference Material Management: Receives, stores, labels and documents reference materials received. Registers the collection and distribution of reference material in the reference materials note book. Registers the collection and distribution of opiates in the reference materials note book. Additional Responsibilities: Coordinates and may assist with the maintenance and repairs of sample storage locations. Qualifications Education: High school / Intermediate Vocational education or other international equivalent. Education/certification for specific equipment or other relevant areas in order to perform the duties. Experience: 2 years of experience. Read, write and speak English; fluent in host country language required. Preferred Education and/or experience: Associates degree in a laboratory related field preferred. Shift: Tuesday - Saturday; typical business hours. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224241
Jan 18, 2020
Pharmaceutical Research Associates, Inc. Lab Sample Receipt Associate - Lenexa, KS US-KS-Lenexa Job ID: 2020-60684 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities Sample Management: Receives, inventories, monitors, documents and stores samples according to appropriate storage conditions. Performs data entry into Watson and other appropriate tracking spreadsheets to account for all specimens received. Informs Project Manager (PM) and Bioanalytical Team Leader (BTL) of sample receipt. Destroys samples and creates appropriate documentation of sample destruction after approval of the PM. Ordering of general laboratory supplies: Orders and tracks general laboratory supplies. Checks receipts of general laboratory supplies and report defects. Processes and register of general laboratory supplies. General Laboratory Support: Coordinates disposal of waste materials. Periodically registers temperatures of freezers and refrigerators. Project Management Support: Inform Project Manager (PM) and Bioanalytical Team Leader (BTL) on receipt of samples. Reference Material Management: Receives, stores, labels and documents reference materials received. Registers the collection and distribution of reference material in the reference materials note book. Registers the collection and distribution of opiates in the reference materials note book. Additional Responsibilities: Coordinates and may assist with the maintenance and repairs of sample storage locations. Qualifications Education: High school / Intermediate Vocational education or other international equivalent. Education/certification for specific equipment or other relevant areas in order to perform the duties. Experience: 2 years of experience. Read, write and speak English; fluent in host country language required. Preferred Education and/or experience: Associates degree in a laboratory related field preferred. Shift: Tuesday - Saturday; typical business hours. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224241
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Lab Analyst (LCMS) - Lenexa, KS US-KS-Lenexa Job ID: 2020-60683 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Who are you? You are a task oriented, analytical and science minded individual. You are a logical thinker who likes all things to be order around you, yet are easily adaptable to change. You strive for perfection, and you are never done learning. You are open to keeping your schedule flexible when there is extra work to be done to meet a deadline. Still here? Wonderful! Because the Lab Analyst is an excellent opportunity to drive your career forward learn from Laboratory Science test and be a part of the evolution of medicine . What will you be doing? The Lab Analyst ensure s appro p ri ate development, validation and use of analytical methods. The lab analyst is also a part of a team which is responsible for quality control within the laboratory processes and supporting the reporting of data from the studies. Daily Tasks may include: Maintaining of equipment, calibration Processing samples and injecting on instruments. Routenty processing samples with different techniques I nterpret ing data processing/reporting results and approve or reject sample analysis Identifying deviations and performing investigation under supervision of a lab analyst level 3 or higher Performs (peer) data review for quality control Has a thorough understanding and complies with GLP and other appropriate regulations Identifies and reports irregularities identified with any aspects of work Economically utilizes materials in operation of daily tasks Ensures on-time task completion to support the overall goal of on-time study completion Assists in the organization and housekeeping of the laboratory Training lab analyst level 1 (before a level 1 lab analyst can train, the lab analyst needs to have minimal 1 year experience) In study planning (daily basis) Understands the scientific principles behind analysis methods utilized Qualifications What do you need to have? Basic laboratory skills Laboratory e ducation (Minimum Requirement) Experience working in a regulated laboratory environment ( GxP ) handling (biological) samples Read, write and speak fluent English; fluent in host country language required. 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. Shift available: Monday - Friday 2:00 p.m. - 11:00 p.m. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224278
Jan 18, 2020
Pharmaceutical Research Associates, Inc. Lab Analyst (LCMS) - Lenexa, KS US-KS-Lenexa Job ID: 2020-60683 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Who are you? You are a task oriented, analytical and science minded individual. You are a logical thinker who likes all things to be order around you, yet are easily adaptable to change. You strive for perfection, and you are never done learning. You are open to keeping your schedule flexible when there is extra work to be done to meet a deadline. Still here? Wonderful! Because the Lab Analyst is an excellent opportunity to drive your career forward learn from Laboratory Science test and be a part of the evolution of medicine . What will you be doing? The Lab Analyst ensure s appro p ri ate development, validation and use of analytical methods. The lab analyst is also a part of a team which is responsible for quality control within the laboratory processes and supporting the reporting of data from the studies. Daily Tasks may include: Maintaining of equipment, calibration Processing samples and injecting on instruments. Routenty processing samples with different techniques I nterpret ing data processing/reporting results and approve or reject sample analysis Identifying deviations and performing investigation under supervision of a lab analyst level 3 or higher Performs (peer) data review for quality control Has a thorough understanding and complies with GLP and other appropriate regulations Identifies and reports irregularities identified with any aspects of work Economically utilizes materials in operation of daily tasks Ensures on-time task completion to support the overall goal of on-time study completion Assists in the organization and housekeeping of the laboratory Training lab analyst level 1 (before a level 1 lab analyst can train, the lab analyst needs to have minimal 1 year experience) In study planning (daily basis) Understands the scientific principles behind analysis methods utilized Qualifications What do you need to have? Basic laboratory skills Laboratory e ducation (Minimum Requirement) Experience working in a regulated laboratory environment ( GxP ) handling (biological) samples Read, write and speak fluent English; fluent in host country language required. 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. Shift available: Monday - Friday 2:00 p.m. - 11:00 p.m. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117224278
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Lab Analyst (Flow Cytometry) - Lenexa, KS US-KS-Lenexa Job ID: 2019-60203 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Who are you? You are a task oriented, analytical and science minded individual. You are a logical thinker who likes all things to be order around you, yet are easily adaptable to change. You strive for perfection, and you are never done learning. You are open to keeping your schedule flexible when there is extra work to be done to meet a deadline. Still here? Wonderful! Because the Lab Analyst is an excellent opportunity to drive your career forward learn from Laboratory Science test and be a part of the evolution of medicine . What will you be doing? The Lab Analyst ensure s appro p ri ate development, validation and use of analytical methods. The lab analyst is also a part of a team which is responsible for quality control within the laboratory processes and supporting the reporting of data from the studies. Daily Tasks may include: Maintaining of equipment, calibration Processing samples and injecting on instruments. Routenty processing samples with different techniques I nterpret ing data processing/reporting results and approve or reject sample analysis Identifying deviations and performing investigation under supervision of a lab analyst level 3 or higher Performs (peer) data review for quality control Has a thorough understanding and complies with GLP and other appropriate regulations Identifies and reports irregularities identified with any aspects of work Economically utilizes materials in operation of daily tasks Ensures on-time task completion to support the overall goal of on-time study completion Assists in the organization and housekeeping of the laboratory Training lab analyst level 1 (before a level 1 lab analyst can train, the lab analyst needs to have minimal 1 year experience) In study planning (daily basis) Understands the scientific principles behind analysis methods utilized Qualifications What do you need to have? Basic laboratory skills Laboratory e ducation (Minimum Requirement) Experience working in a regulated laboratory environment ( GxP ) handling (biological) samples Read, write and speak fluent English; fluent in host country language required. 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. Shifts available: Monday - Friday 2:00 p.m. - 11:00 p.m. Tuesday - Saturday 10:00 a.m. - 7:00 p.m. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117094068
Jan 15, 2020
Pharmaceutical Research Associates, Inc. Lab Analyst (Flow Cytometry) - Lenexa, KS US-KS-Lenexa Job ID: 2019-60203 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Who are you? You are a task oriented, analytical and science minded individual. You are a logical thinker who likes all things to be order around you, yet are easily adaptable to change. You strive for perfection, and you are never done learning. You are open to keeping your schedule flexible when there is extra work to be done to meet a deadline. Still here? Wonderful! Because the Lab Analyst is an excellent opportunity to drive your career forward learn from Laboratory Science test and be a part of the evolution of medicine . What will you be doing? The Lab Analyst ensure s appro p ri ate development, validation and use of analytical methods. The lab analyst is also a part of a team which is responsible for quality control within the laboratory processes and supporting the reporting of data from the studies. Daily Tasks may include: Maintaining of equipment, calibration Processing samples and injecting on instruments. Routenty processing samples with different techniques I nterpret ing data processing/reporting results and approve or reject sample analysis Identifying deviations and performing investigation under supervision of a lab analyst level 3 or higher Performs (peer) data review for quality control Has a thorough understanding and complies with GLP and other appropriate regulations Identifies and reports irregularities identified with any aspects of work Economically utilizes materials in operation of daily tasks Ensures on-time task completion to support the overall goal of on-time study completion Assists in the organization and housekeeping of the laboratory Training lab analyst level 1 (before a level 1 lab analyst can train, the lab analyst needs to have minimal 1 year experience) In study planning (daily basis) Understands the scientific principles behind analysis methods utilized Qualifications What do you need to have? Basic laboratory skills Laboratory e ducation (Minimum Requirement) Experience working in a regulated laboratory environment ( GxP ) handling (biological) samples Read, write and speak fluent English; fluent in host country language required. 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. Shifts available: Monday - Friday 2:00 p.m. - 11:00 p.m. Tuesday - Saturday 10:00 a.m. - 7:00 p.m. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117094068
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Medical Research Associate - Second Shift - Lenexa, KS US-KS Job ID: 2019-58756 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities 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! Clinic 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 Read, write, and speak English; fluent in host country language required. 1-2 years work experience in a medical or clinical field. 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 preferred. Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, Emergency Medical Technician, Laboratory Technician preferred. BLS/Phlebotomist Certification. Two years of equivalent work experience preferred. Shift: Must be available to work an 8-hour shift between the hours of 3:00 p.m. - midnight. Additionally, must commit to working 1 weekend day per week or every other weekend. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117094245
Jan 15, 2020
Pharmaceutical Research Associates, Inc. Medical Research Associate - Second Shift - Lenexa, KS US-KS Job ID: 2019-58756 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities 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! Clinic 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 Read, write, and speak English; fluent in host country language required. 1-2 years work experience in a medical or clinical field. 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 preferred. Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, Emergency Medical Technician, Laboratory Technician preferred. BLS/Phlebotomist Certification. Two years of equivalent work experience preferred. Shift: Must be available to work an 8-hour shift between the hours of 3:00 p.m. - midnight. Additionally, must commit to working 1 weekend day per week or every other weekend. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117094245
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. ETL Developer US-KS-Lenexa Job ID: 2019-60155 Type: US-Midwest # of Openings: 1 Category: Information Technology PRA Health Sciences Overview ETL Developer Do you want to watch clinical technology 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 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? You are a forward thinker. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be an ETL Engineer; you want to change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number…a place you love working. Still here? Good. If this is you, we’d really like to meet you. Responsibilities We’re taking a fresh approach at ways that technology and analytics can empower those working in the clinical lifecycle and shape the future of clinical development. This role will be responsible for: Development and maintenance of ETLs and reports, including requirements analysis, design, implementation, testing, deployment and documentation. Documenting, studying, and analyzing current business processes, and determining improvements. Qualifications Required: 3+ years of ETL experience. 3+ years of development experience with Informatica PowerCenter. Excellent knowledge of SQL and PL/SQL with the ability to extract, manipulate and integrate enterprise data, developing reports and expanding reporting capability utilizing SQL backend mining tools. Excellent verbal and written communication skills. Bachelor’s degree or international equivalent. Ability to perform comfortably in a fast-paced, deadline-oriented work environment. 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. Preferred: Experience working on ETL integration projects Database Design exp. ETL Solution Design exp. (design of ETL workflows, without much guidance) DataStage Talend SSIS PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117053640
Jan 13, 2020
Pharmaceutical Research Associates, Inc. ETL Developer US-KS-Lenexa Job ID: 2019-60155 Type: US-Midwest # of Openings: 1 Category: Information Technology PRA Health Sciences Overview ETL Developer Do you want to watch clinical technology 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 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? You are a forward thinker. You are an innovator that refuses to settle. You want to push the boundaries and change not just what it means to be an ETL Engineer; you want to change the future. You want to learn from the best, grow your knowledge and your skill set, and you want to build your career. You want to use the latest technology and tools in the industry to push the momentum of an already growing company forward. You want to find a balance that still lets you be, well, you. Most of all, you want to do it in a place where you’re more than an employee number…a place you love working. Still here? Good. If this is you, we’d really like to meet you. Responsibilities We’re taking a fresh approach at ways that technology and analytics can empower those working in the clinical lifecycle and shape the future of clinical development. This role will be responsible for: Development and maintenance of ETLs and reports, including requirements analysis, design, implementation, testing, deployment and documentation. Documenting, studying, and analyzing current business processes, and determining improvements. Qualifications Required: 3+ years of ETL experience. 3+ years of development experience with Informatica PowerCenter. Excellent knowledge of SQL and PL/SQL with the ability to extract, manipulate and integrate enterprise data, developing reports and expanding reporting capability utilizing SQL backend mining tools. Excellent verbal and written communication skills. Bachelor’s degree or international equivalent. Ability to perform comfortably in a fast-paced, deadline-oriented work environment. 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. Preferred: Experience working on ETL integration projects Database Design exp. ETL Solution Design exp. (design of ETL workflows, without much guidance) DataStage Talend SSIS PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117053640
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Associate Business Intelligence Developer US-KS-Lenexa Job ID: 2019-60153 Type: US-Midwest # of Openings: 1 Category: Information Technology PRA Health Sciences Overview Associate BI Developer (Entry-level) Data Analyst 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 90+ 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. Overview: The Data Analyst develops effective ways for stakeholders to view, use, and understand large complex sets of data, typically through visual representation. They design, develop, and enhance reports, dashboards, and visualizations for internal and/or external customers. Responsibilities Responsibilities: Understands, analyzes, designs, develops and documents Business Intelligence deliverables Translates business requirements into technical requirements to implement reports and dashboards. Collaborates with stakeholders to design, develop, and maintain ongoing metrics, reports, analyses and dashboards to drive key business decisions Provides training and support to end users to ensure full understanding and full utilization of created tools Ensures business intelligence availability through support functions and thorough testing. Assists in design, implementing, and maintaining BI reports/ dashboards/ visualizations Assists with creation of data sets and data interfaces for reporting and interactive dashboard. Assists in building reports, dashboards and visualizations using BI tools Assist in testing created reports/tools/ visualizations prior to release Provide s support for training end users on created solutions Provide status reports to management team Escalates project issues when necessary. Qualifications Qualifications: Bachelor’s Degree or international equivalent 0-2+ years of relevant experience Knowledge of dashboard flow, interactivity design and sizing Ability to define and translate requirements for effective BI solutions. Good report development skills Good analytical and problem-solving skills Good organizational, interpersonal, verbal, and written communication skills 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. Preferred: Strong SQL Skills Experience working with Oracle and/or SQL Servers Exposure to ‘Big Data’ analytics and reporting PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117053655
Jan 13, 2020
Pharmaceutical Research Associates, Inc. Associate Business Intelligence Developer US-KS-Lenexa Job ID: 2019-60153 Type: US-Midwest # of Openings: 1 Category: Information Technology PRA Health Sciences Overview Associate BI Developer (Entry-level) Data Analyst 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 90+ 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. Overview: The Data Analyst develops effective ways for stakeholders to view, use, and understand large complex sets of data, typically through visual representation. They design, develop, and enhance reports, dashboards, and visualizations for internal and/or external customers. Responsibilities Responsibilities: Understands, analyzes, designs, develops and documents Business Intelligence deliverables Translates business requirements into technical requirements to implement reports and dashboards. Collaborates with stakeholders to design, develop, and maintain ongoing metrics, reports, analyses and dashboards to drive key business decisions Provides training and support to end users to ensure full understanding and full utilization of created tools Ensures business intelligence availability through support functions and thorough testing. Assists in design, implementing, and maintaining BI reports/ dashboards/ visualizations Assists with creation of data sets and data interfaces for reporting and interactive dashboard. Assists in building reports, dashboards and visualizations using BI tools Assist in testing created reports/tools/ visualizations prior to release Provide s support for training end users on created solutions Provide status reports to management team Escalates project issues when necessary. Qualifications Qualifications: Bachelor’s Degree or international equivalent 0-2+ years of relevant experience Knowledge of dashboard flow, interactivity design and sizing Ability to define and translate requirements for effective BI solutions. Good report development skills Good analytical and problem-solving skills Good organizational, interpersonal, verbal, and written communication skills 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. Preferred: Strong SQL Skills Experience working with Oracle and/or SQL Servers Exposure to ‘Big Data’ analytics and reporting PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI117053655
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Bioanalytical Lab Scientist - Lenexa, KS US-KS-Lenexa Job ID: 2020-60414 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Sample Analysis and Assay Validation Provides key assay input to the research project and assay validation to ensure successful execution Assay troubleshooting May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel. Method Development Develops assays independently but with team interaction Develops new scientific approaches to method development and communicates these to the global science team so that they can be broadly implemented. Mentoring of more junior scientists and advising operation on developed methods. Reviews and approves data of other scientists. Communicates with team members and management regarding project status, purpose, scheduling, problems, etc. Utilizes standard approach for method development Communicates and/or participates in communication with clients regarding project status. Scientific Maintain knowledge and skill in all techniques where you perform your work. Provide scientific input to management and BD about new technology investments and lines of service. Discusses scientific results with sponsors together with project manager Promotes PRA utilizing their scientific skills through scientific communication such as external publication of posters and journal articles. Perform R&D projects Training of technicians on technical aspects Quality and Timely Work Execution Takes initiative in process development and SOP/WI writing. Legible, logical and reproducible documentation of all experimentation. Develops and communicates an accurate estimate of time frame for project completion. Has a thorough understanding and complies with GLP and other appropriate regulations Develops rugged and economical assays Performs data review of other scientists work. Mentor and train staff on scientific topics. Qualifications Education BSc in Science with relevant experience. Experience Read, write and speak fluent English; fluent in home country language required. 3-5 years as a Scientist in a relevant Laboratory Preferred BS + 5 years of experience PhD with applicable research in a relevant Scientific field. Presenter/Publisher in Regulated relevant Field PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI116849301
Jan 05, 2020
Pharmaceutical Research Associates, Inc. Bioanalytical Lab Scientist - Lenexa, KS US-KS-Lenexa Job ID: 2020-60414 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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 Bioanalytical Labs, with locations in Lenexa, KS USA and Assen, Netherlands, EU. We are part of the 16,000+ employees strong for PRA Health Sciences, operating in more than 90 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. Responsibilities Sample Analysis and Assay Validation Provides key assay input to the research project and assay validation to ensure successful execution Assay troubleshooting May perform and document maintenance, trouble-shooting and repairs on advanced instrumentation with support of service engineers or other trained supervisory personnel. Method Development Develops assays independently but with team interaction Develops new scientific approaches to method development and communicates these to the global science team so that they can be broadly implemented. Mentoring of more junior scientists and advising operation on developed methods. Reviews and approves data of other scientists. Communicates with team members and management regarding project status, purpose, scheduling, problems, etc. Utilizes standard approach for method development Communicates and/or participates in communication with clients regarding project status. Scientific Maintain knowledge and skill in all techniques where you perform your work. Provide scientific input to management and BD about new technology investments and lines of service. Discusses scientific results with sponsors together with project manager Promotes PRA utilizing their scientific skills through scientific communication such as external publication of posters and journal articles. Perform R&D projects Training of technicians on technical aspects Quality and Timely Work Execution Takes initiative in process development and SOP/WI writing. Legible, logical and reproducible documentation of all experimentation. Develops and communicates an accurate estimate of time frame for project completion. Has a thorough understanding and complies with GLP and other appropriate regulations Develops rugged and economical assays Performs data review of other scientists work. Mentor and train staff on scientific topics. Qualifications Education BSc in Science with relevant experience. Experience Read, write and speak fluent English; fluent in home country language required. 3-5 years as a Scientist in a relevant Laboratory Preferred BS + 5 years of experience PhD with applicable research in a relevant Scientific field. Presenter/Publisher in Regulated relevant Field PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI116849301
Pharmaceutical Research Associates, Inc.
Lenexa, KS, USA
Pharmaceutical Research Associates, Inc. Phlebotomist - Medical Research Associate - Full Time - Lenexa, KS US-KS Job ID: 2019-58758 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities 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! Clinic 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 Read, write, and speak English; fluent in host country language required. 1-2 years work experience in a medical or clinical field. 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 preferred. Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, Emergency Medical Technician, Laboratory Technician preferred. BLS/Phlebotomist Certification. Two years of equivalent work experience preferred. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI116819487
Jan 04, 2020
Pharmaceutical Research Associates, Inc. Phlebotomist - Medical Research Associate - Full Time - Lenexa, KS US-KS Job ID: 2019-58758 Type: US-Midwest # of Openings: 1 Category: Early Development Services 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. Responsibilities 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! Clinic 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 Read, write, and speak English; fluent in host country language required. 1-2 years work experience in a medical or clinical field. 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 preferred. Medical Assistant, Certified Nursing Assistant, Certified Medication Aide, Telemetry Technician, Emergency Medical Technician, Laboratory Technician preferred. BLS/Phlebotomist Certification. Two years of equivalent work experience preferred. PRA is an EEO/AA employer and is committed to providing opportunities to minorities, women, veterans and individuals with disabilities. PI116819487
We’ll float your boat. The Pay - Competitive mileage rates - $1,200 to $1,500 per week - $700 safety and fuel bonus per quarter The Benefits - Cigna health, dental, and vision - Driver premiums paid mostly by Voyager - Paid vacation at one year The Advantages - Weekly home time - Dedicated dispatchers - Family company The Routes - Dedicated regional lanes - 10-13 thousand miles a month! - 11 western states The Equipment - Modern, shipshape equipment - no leaks! - Dry vans and flatbeds - On-site maintenance The Qualifications - CDL A + 2 years experience - No major preventable accidents or violations in 3 years - No DUI/DWI Apply Here! DriveVoyager.com or 855.776.5144 CDL-A Drivers Has finding the right truckline felt like paddling upstream? Then turn a corner and join our fleet. We'll keep you smooth-sailing all week and docked at home on weekends. . PI116764379
Jan 02, 2020
We’ll float your boat. The Pay - Competitive mileage rates - $1,200 to $1,500 per week - $700 safety and fuel bonus per quarter The Benefits - Cigna health, dental, and vision - Driver premiums paid mostly by Voyager - Paid vacation at one year The Advantages - Weekly home time - Dedicated dispatchers - Family company The Routes - Dedicated regional lanes - 10-13 thousand miles a month! - 11 western states The Equipment - Modern, shipshape equipment - no leaks! - Dry vans and flatbeds - On-site maintenance The Qualifications - CDL A + 2 years experience - No major preventable accidents or violations in 3 years - No DUI/DWI Apply Here! DriveVoyager.com or 855.776.5144 CDL-A Drivers Has finding the right truckline felt like paddling upstream? Then turn a corner and join our fleet. We'll keep you smooth-sailing all week and docked at home on weekends. . PI116764379