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...

The Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

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 Clin...

Collaborate with the clinical research team to ensure timely prescreening of potential subjects and active cancer patients for all available clinical trials. Knowledge of clinical research coordinator...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...

The Clinical Research Coordinator Bilingual Mandarin/English (CRC Bilingual Mandarin/English) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not lim...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...

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...

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 Clin...

As a Research Coordinator, you will be an integral member of our research team, and support the conduct of an NIH-funded randomized trial to investigate the effects of an information-sharing intervent...

A Clinical Research Coordinator (CRC) I position is currently available to support our Multiple Myeloma Program within the Tisch Cancer Institute. Assists in the activities related to clinical researc...

As a Research Coordinator, you will be an integral member of our research team, and support the conduct of an NIH-funded randomized trial to investigate the effects of an information-sharing intervent...

The Clinical Research Coordinator assists in the daily activities of clinical research studies, obtains informed consent; collects, maintains and organizes study information. Assists in the activities...

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...

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...

The Clinical Research Coordinator is an entry human subjects researcher, responsible for conducting and assisting in clinical research studies under the supervision of the Principal Investigator or se...

Conducts routine and standardized human subjects research using appropriate research or interview techniques specific to subject matter of the research project, under direct supervision of the Princip...

The Clinical Research Coordinator (CRC) is an entry human subjects researcher, responsible for assisting the lab leadership (including but not limited to CRC I), in clinical research studies. Conducts...

A Clinical Research Coordinator (CRC) I position is currently available to support our Multiple Myeloma Program within the Tisch Cancer Institute. Assists in the activities related to clinical researc...

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...

Rutgers, The State University of New Jersey, is seeking a Clinical Research Coordinator for the Clinical Research Center at the Robert Wood Johnson Medical School. Under the direction of the CRC Nurse...

We 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...

We 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...

The Research Coordinator administers and coordinates research studies and associated activities under the direction of the Office of Research and Grants Administration. The Research Coordinator will a...

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...

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...

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...

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...

Adheres to good clinical practice, and complies with regulatory and grant agency requirements, and study protocol; maintains study records and collaborates with the institutional review board as neces...

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 ...

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 ...

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 ...

A minimum of four years of Clinical Research Coordinator experience, including research in investigator-initiated research and IND/IDE trials. The Rockefeller University, the world's premier Research ...

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...