Full-Time

Clinical Research Coordinator A/B

Epidemiology Division

Posted on 5/9/2026

University of Pennsylvania

University of Pennsylvania

No salary listed

Philadelphia, PA, USA

Hybrid

Requires in-person study visits at least 4 days per week.

Category
Biology & Biotech (1)
Requirements
  • Bachelor's degree required and 1-2 years of related experience (or equivalent combination of education and experience) for Clinical Research Coordinator A
  • Bachelor's degree required and 2-3 years of related experience (or equivalent combination of education and experience) for Clinical Research Coordinator B
  • Regulatory experience (for B) and chart review experience preferred
  • REDCap experience preferred
  • Effective problem-solving abilities; effective communication and writing skills; strong organizational and time management skills; flexible, with the ability to manage multiple priorities simultaneously; strong attention to detail; demonstrated ability to work as part of a team, as well as independently; knowledge of human research protection regulations; highly reliable
  • Strong interpersonal skills with the ability to interact with patients in a healthcare setting
Responsibilities
  • Screening, recruiting, and consenting patients according to protocol
  • Chart review to confirm eligibility
  • Scheduling and conducting patient study visits
  • Collecting study data, completing case report forms, entering data into study databases and resolving data entry errors/queries
  • Communicating with study team members and patients
  • Collecting and processing (if needed) study specimens
  • Participating in study team meetings
  • Showing vigilance in patient safety, protocol compliance, and data integrity
  • Adhering to all University of Pennsylvania and Good Clinical Practice guidelines
  • Establish workflows and methods to operationalize protocols
  • Regularly prepare, draft, and submit regulatory correspondences
  • Mentor/train less experienced research staff in the completion of their duties
  • Participate in the development of protocols and data collection instruments
  • Less supervision and more independent judgment in managing assigned research studies
Desired Qualifications
  • REDCap experience preferred
  • Regulatory and chart review experience preferred
University of Pennsylvania

University of Pennsylvania

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