Clinical Trials Coordinator

3 days ago


New Brunswick, New Jersey, United States Rutgers The State University Full time
Job Responsibilities
The Research Nurse Clinician will play a crucial role in the success of our clinical trials program. Key responsibilities include:
  • Collaborating with the Protocol Activation office to initiate and activate all new clinical trial protocols assigned utilizing Oncore Study-start up task list.
  • Preparing and reviewing study tools such as study binders, medication diaries, eligibility checklists, and flow sheets (as required).
  • Verifying Scientific Review Board (SRB), Institutional Review Board (IRB), data collection plans, and finance/contract approvals prior to study activation.
  • Collaborating with the clinical research team to ensure timely prescreening of potential subjects and active cancer patients for all available clinical trials.
  • Reviewing patient charts and medical history to confirm protocol eligibility and obtaining source documents (i.e., medical record documentation) as needed.

About the Opportunity
This is an exceptional opportunity to join a renowned research institution and contribute to the advancement of cancer care. With a competitive salary and comprehensive benefits package, we offer a supportive work environment that fosters growth and development. If you are a motivated and detail-oriented individual with a passion for oncology research, we encourage you to apply.

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