Clinical Research Coordinator
Job Description Summary
Serves as a resource for best practices in managing major clinical trials, working independently with minimal supervision. Provides guidance on both study and device trials, oversees implementation of new protocols, and supports regulatory compliance. Coordinates with investigators, sponsors, and regulatory staff to resolve challenges, ensure timely IRB submissions, and support effective trial operations.
Job Description
Job Responsibilities
- Coordinate clinical research for Dr. Al-Aswad lab.
- Recruit, consent and screen patients according to protocol
- Schedule patient visits and any necessary testing. Monitor patients per protocol requirements and ensure adherence to protocol requirements
- Organize and maintain all required documentation- including source documentation, case report forms, and research charts. Collect, review and report study data, Complete case report forms and resolve data queries
- Participate in the initiation, monitoring, audit, and close-out visits. Participate in study team meetings disease site group meetings, and ongoing protocol training/compliance meetings
- Develop/maintain study specific case report forms and source document tools
- Other duties and responsibilities as assigned
Position contingent upon funding.
Qualifications
- Bachelor of Science and 4 to 6 years of experience or equivalent combination of education and experience is required.
Job Location - City, State
Philadelphia, Pennsylvania
Department / School
Perelman School of Medicine
Pay Range
$62,000.00 - $65,000.00 Annual Rate
To apply, visit https://wd1.myworkdaysite.com/en-US/recruiting/upenn/careers-at-penn/job/Scheie-Eye-Institute/Clinical-Research-Coordinator_JR00118154
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