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...

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...

Under the direction of the Assistant Dean for Clinical Research, the Clinical Research Coordinator III provides essential research and program support to the Director, Program Manager and other profes...

Clinical 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...

Working 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...

Working 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...

The 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...

Clinical 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...

Clinical 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...

Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...

Functions independently in a clinical research setting and responsible for the complete coordination of assigned clinical research protocols from national research agencies and pharmaceutical corporat...

Assist in the conduct of clinical studies as specified by the study protocol under the supervision of designated Principal Investigator and departmental management. Perform department specific procedu...

Eurofins is the global leader in food, environment, pharmaceutical and cosmetic product testing and in agroscience Contract Research Organisation services. Eurofins is one of the market leaders in cer...

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...

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...

Experience in clinical research, clinical operations, or billing compliance.

Reports 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...

Reports 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. PR...

Minimum 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...

Demonstrated 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...

SOCRA-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...

SOCRA-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...

Minimum 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...

SOCRA-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...

Minimum 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...

Adheres 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 ...

Adheres 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 ...

Adheres 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 ...

Coordinates 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...

In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Adheres to good clinical practice, and complies with regulatory a...

In research projects, oversees recruitment of subjects, implementation of study procedures, and the collection and processing of data. Adheres to good clinical practice, and complies with regulatory a...

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 ...

Minimum 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...

Position 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 ...

Position 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 ...

The 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...

Position 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...

Position 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...

Minimum 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...