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 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 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 moreWe are seeking a motivated and detail-oriented Clinical Research Coordinator to join our team in Livingston, NJ. Minimum of 1 year experience as a Clinical Research Coordinator. AM – 4:00 PM (fl...
read moreWe are seeking a motivated and detail-oriented Clinical Research Coordinator to join our team in Livingston, NJ. Minimum of 1 year experience as a Clinical Research Coordinator. AM – 4:00 PM (fl...
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 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 moreEurofins is one of the market leaders in certain testing and laboratory services for genomics, discovery pharmacology, forensics, advanced material sciences and in the support of clinical studies, as ...
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...
read moreReports to Director of Clinical Trials or Clinical Research Nurse Lead: Collaborates with departmental leadership and research staff in the coordination of all aspects of clinical research studies. Fu...
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 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 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 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 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 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 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 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 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 moreThe Laboratory Coordinator plays a crucial role in the execution of clinical lab testing protocols, and new assay and new instruments validation and verification. The coordinator manages the labs qual...
read moreAssist in the conduct of clinical trials as specified by the study protocol under the supervision of designated Principal Investigator and departmental management.
Assist 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 moreThe 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 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 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 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 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...
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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