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Clinical trial coordinator jobs in Trenton nj

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Senior Clinical Research Coordinator ATLANTIC CITY, NJ, UNITED STATES Senior Clinical Research Coordinator Location: Atlantic City, NJDuration: 8-9 monthsDescription: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as well as...
Clinical - Rheumatology Review Group Eligibility Liaison - Hybrid! MADISON, NJ, UNITED STATES ...experience as a Clinical Trial Assistant, Clinical Trial Specialist or Clinical Team Manager would be preferred. Must Have: 2 to 5 years of experience in clinical research (industry, academic or study site is acceptable).Proficiency in Microsoft Office software and Electronic Data...
Clinical - Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data. Position Summary /Objective \" Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. \" Manage communication of participant status with the RRG...
Looking for Clinical Trial Coordinator jobs in Trenton Nj? Top Salaries! Full time, part time and contract. TRENTON NJ Visit PerfectJobs4U UK for the widest selection of top UK jobs. Full time, part time and work from home roles.
Clinical - Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data. Position Summary /Objective \" Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. \" Manage communication of participant status...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...site communication and clinical/study data coordination and tracking.Manage communication of participant status with the RRG via email and REL progress tracker.Completes training and remains current with RRG processes to respond to a site s questions related to Screening EligibilityWork...
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Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data. Position Summary /Objective \" Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. \" Manage communication of participant status with the RRG...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES 12 months ContractJob Title: Rheumatology Review Group (RRG) Eligibility LiaisonFunctional Area Description: The RRG Eligibility Liaison (REL) employs scientific and technical expertise to track, coordinate and enforce the timely delivery of quality clinical/study data.Position Summary...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data. Position Summary /Objective - Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. - Manage communication of...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data. Position Summary /ObjectiveResponsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking.Manage communication of participant status with the RRG via...
Rheumatology Review Group (RRG) Eligibility Liaison MADISON, NJ, UNITED STATES Job Title: Rheumatology Review Group (RRG) Eligibility LiaisonLocation: Madison, NJ 07940Duration: 12 MonthsMust be able to work onsite 50% of the time at Madison, NJ or Princeton Pike, NJ Must Have List:\" 2 to 5 years of experience in clinical research (industry, academic or study site...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data.Position Summary /Objective \" Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. \" Manage communication of participant status with the...
Rheumatology Review Group Eligibility Liaison MADISON, NJ, UNITED STATES ...delivery of quality clinical/study data.Position Summary /Objective Responsible for ensuring site participants in screening are ready for RRG review through site communication and clinical/study data coordination and tracking. Manage communication of participant status...

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Clinical Research Coordinator URBANA, ILLINOIS, UNITED STATES The Clinical Research Coordinator (CRC) is a specialized research professional that facilitates and coordinates the daily activities of a clinical trial and plays a critical role in the conduct of the study. The CRC conducts clinical trials using good clinical/scientific practices under the...
RN - Cardiology - Clinical Trial Research - FT Day CARMEL, INDIANA, UNITED STATES ...Responsibilities Lead clinical research projects via study protocols and provide direct patient care for study participants. Assist with the preparation, submission and management of internal/external compliance documentation at all stages of the research project. Assist with the selection...
Clinical Research Coordinator II Registered Nurse WINSTON-SALEM, NORTH CAROLINA, UNITED STATES Overview The RN clinical research coordinator (CRC) is a clinical research professional working under the direction of their Novant Health leader and the principal investigator. Clinical research coordinators facilitate and coordinate the daily clinical trial activities and play a critical role in...
HYBRID: Research Regulatory Coordinator URBANA, ILLINOIS, UNITED STATES The Research Regulatory Coordinator is a specialized research professional that facilitates and coordinates the regulatory aspects of a clinical trial and plays a critical role in the conduct of research at Carle. This role is responsible for preparing, completing, and submitting required forms and...
Senior Clinical Research Coordinator DEERFIELD, IL, UNITED STATES Senior Clinical Research Coordinator Location: Deerfield, IL/ Chicago, IL/HybridDuration: 12 months with possible contract to hire/ with possible extensionDescription: The Senior Clinical Research Coordinator (CRC) is responsible for managing and overseeing the day-to-day operations of...
Senior Clinical Research Coordinator KANSAS CITY, MO, UNITED STATES Senior Clinical Research CoordinatorDescription:Summary:One of our Pharmaceutical Client is looking for Senior Clinical Research Coordinator (CRC) who will be responsible for managing and overseeing the day-to-day operations of clinical trials, recruiting and screening study participants, as...
Clinical Trial Associate CHICAGO, IL, UNITED STATES The Alliance for Clinical Trials in Oncology Foundation (Foundation) is a foundation created to enhance and expand the ability of the Alliance for Clinical Trials in Oncology (Alliance) to conduct cancer clinical research and address important treatment questions through large-scale clinical...
Clinical Research Coordinator RALEIGH, NC, UNITED STATES Job DescriptionThe Clinical Research Coordinator (CRC) is a specialized research professional working with and under the guidance of the clinical research site management and Principal Investigator (PI). While the PI is primarily responsible for the overall conduct of the clinical trial, the CRC...
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