CCRP (Certified Clinical Research Professional) or ACRP (Association of Clinical Research Professionals) certification. We are seeking a highly motivated and detail-oriented Clinical Research Data Coo...
read moreCCRP (Certified Clinical Research Professional) or ACRP (Association of Clinical Research Professionals) certification. We are seeking a highly motivated and detail-oriented Clinical Research Data Coo...
read moreThe Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Bachel...
read moreWorking under the direction of the Principal Investigator (PI), responsible for the overall coordination and administration of daily activities of ICR clinical trials. Oversees the research process fr...
read moreWithin the Department of Neurology’s Clinical Research Office and reporting to the Research manager with a focus on movement disorders trials, the Clinical Research Coordinator (CRC) will lead efforts...
read moreThe Oncology CRC performs study coordination tasks under the direction of the principal investigator/treating investigator, under the supervision of the CTO management/leadership and works closely wit...
read moreThe Clinical Research Coordinator (CRC) will report to the Associate Chief of Genetics Clinical Operations and under the direction of the clinical Principal Investigator (PI) on multiple ongoing resea...
read moreServes as a supporting clinical research coordinator to CRC/CRN II and CRC/CRN III for highly complex Manages, implements, and evaluates all aspects of clinical trial conduct including study initiatio...
read moreClinical Research Coordinator, you will be responsible for coordinating and facilitating the daily activities that play a critical role of the clinical studies according to the protocol, Good Clinical...
read moreFunctions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...
read moreExperience in clinical research, clinical operations, or billing compliance.
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...
read moreExperience in clinical research, clinical operations, or billing compliance.
SOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Along with clinical research nurses, ma...
read moreCoordinates the synchronization of research activities within the ARJR service under the direction of the ARJR Director and serves as a liaison between the clinicians, research staff, and other resear...
read moreCoordinates the synchronization of research activities within the ARJR service under the direction of the ARJR Director and serves as a liaison between the clinicians, research staff, and other resear...
read moreDemonstrated experience in clinical research coordination or related roles, with a strong understanding of research. Join our dynamic pulmonology research team as a Research Coordinator, where you wil...
read moreDemonstrated experience in clinical research coordination or related roles, with a strong understanding of research. Join our dynamic pulmonology research team as a Research Coordinator, where you wil...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). Minimum of 2 years experience in a Seni...
read morePart-Time Clinical Research Coordinator (12 hours/week). Minimum of two years in a Clinical Research Coordinator role. This is a short term contract position and requires previous clinical research ex...
read morePart-Time Clinical Research Coordinator (12 hours/week). Minimum of two years in a Clinical Research Coordinator role. This is a short term contract position and requires previous clinical research ex...
read moreMinimum of three years in a Study Coordinator or Clinical Research Coordinator role. Oncology Clinical Research Coordinator. This is a contract position and requires previous Oncology clinical researc...
read moreAs part of a multi-disciplinary research team in transplant surgery and related research, the Research Assoc will be responsible for her/his own portfolio of clinical research projects including, as a...
read moreThe Clinical Research Coordinator II (CRC II) is responsible for providing research services to patients participating in clinical trials within Yale Cancer Center Clinical Trials Office (CTO). Bachel...
read moreUnder the direction of the Associate Director and RN Manager, the Coordinator 4 leads the research team in the execution of trials within the scope of the established study protocol. Demonstrated owne...
read moreSOCRA-Certified Clinical Research Professional (CCRP) and/or Certified Clinical Research Associate (CCRA) and/or Certified Clinical Research Coordinator (CCRC). In collaboration with the principal inv...
read moreWithin the Department of Neurology’s Clinical Research Office and reporting to the Research manager, the Clinical Research Coordinator (CRC) will lead efforts in an NIH funded grant studying seizure f...
read moreMinimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...
read moreAdheres to good clinical practice, and complies with regulatory and grant agency requirements; follows protocol as developed and keeps investigator or supervisor informed of developments. Coordinates ...
read moreCoordinates and monitors research trials; actively oversees the recruitment of study participants. Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and st...
read moreAssist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.
The Clinical Research Coordinator I will be the point person for multiple research projects and help establish, track, oversee, and monitor neuroimaging acquisition protocols, data transfer, and data ...
read moreWork Week: Standard (M-F equal number of hours per day) Posting Position Title: Clinical Research Coordinator 1 University Job Title: Clinical Research Coordinator Preferred Education, Experience and ...
read moreMinimum of 2 or more years of experience in clinical research as a Clinical Research Coordinator, with experience in patient recruiting/screening/consenting/retention; activation; regulatory complianc...
read morePosition Summary Working in the Division of General Medicine under the direction of the Principal Investigator, the Coordinator will provide coordination and data collection in NIH-sponsored research ...
read moreThe Clinical Research Coordinator is an active participant in the coordination of critical care and resuscitation research studies from research planning to completion of studies. The Clinical Researc...
read morePosition Summary The Clinical Research Coordinator (CRC) will provide support for research activities in the Division of Nephrology. Responsibilities Obtain informed consent Organize and conduct basel...
read moreMinimum of 1 to 2 years of experience in Clinical Research as a Clinical Research Coordinator, with experience in patient recruiting/pre-screening/consenting/retention; activation; regulatory complian...
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