Clinical Research Coordinator B (Surgery Research Administration)
This position's primary function is to facilitate, promote, and ensure good clinical practice in the conduct of all research protocols in the Department/Center. Independently manages different phases of complex clinical trials and mentors coordinators and research assistants. Works with partnering institutions and creates multi-center budgets and manages expenses. Participates in study team meetings, disease site group meetings, and ongoing protocol training/compliance meetings. Supports in the monitoring of external sites and assists in the management of multisite trials.
Job Description
- Prepare and process all Institutional Review Board (IRB) through the IRB and other regulatory groups as appropriate including initial submissions, amendments, continuing reviews, adverse events and serious adverse events
- Coordinate, organize and maintain all documentation required by sponsor or CRO (case report forms, source documentation, study and regulatory binders, subject binders)
- Assist in the coordination of Phase I-IV clinical trials
- Participate in the conduct of study audits by sponsors, CRO's, the FDA and other entities as required.
- Schedule patient visits and any necessary testing.
- Adhere to all University of Pennsylvania, ICF, and FDA guidelines.
- Process and ship blood, urine and tissue as required per trial
- Conduct initiation, monitoring and closeout visits with sponsors and/or CROs
- Ensure proper screening and enrollment of all study participants, including administering informed consent and confirming subject study eligibility prior to participation
- Other duties and responsibilities as assigned
Qualifications
Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
This position is contingent on grant funding.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$52,500.00 - $52,661.00 Annual Rate
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