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...

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...

Oversees the research process from inception to completion and prepares and organizes the documentation and files pertaining to a study; coordinates the activities of the investigators and the study p...

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...

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. PR...

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...

Coordinates 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...

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...

Join our dynamic pulmonology research team as a Research Coordinator, where you will contribute to. Demonstrated experience in clinical research coordination or related roles, with a strong understand...

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...

As a Clinical Research Nurse, you will play a crucial role in initiating and activating clinical trial protocols, ensuring adherence to regulatory and institutional standards, and providing high-quali...

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...

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...

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...

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...

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...

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...

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 ...

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...

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...