Full-Time

Clinical Research Coordinator

Updated on 9/3/2026

University of Pennsylvania

University of Pennsylvania

Ivy League university in Philadelphia, PA

Compensation Overview

$46.5k - $56.3k/yr

Philadelphia, PA, USA

In Person

Bachelor's

Category
Biology & Biotech (1)
Required Skills
Medication Administration
Data Analysis

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Requirements
  • CRC-A requires a Bachelor of Science and 1 to 2 years of experience, or an equivalent combination of education and experience.
  • CRC-B requires a Bachelor of Science and 2 to 3 years of experience, or an equivalent combination of education and experience.
  • Adhere to University of Pennsylvania, ICF, and Food and Drug Administration guidelines.
  • Possess in-depth knowledge of federal regulations and guidance documents for clinical studies and human subject protection.
Responsibilities
  • Coordinate and conduct clinical studies, including subject recruitment, informed consent, chart maintenance, and data entry.
  • Coordinate Institutional Review Board submissions and renewals in accordance with Food and Drug Administration and Institutional Review Board guidelines.
  • Ensure compliance with protocols and regulatory requirements by collecting, recording, and maintaining data and source documentation.
  • Oversee study preparation and blood sample processing and analysis.
  • Manage databases and conduct database analysis.
  • Order and stock supplies and maintain equipment.
  • Educate patients and family members.
  • Prepare and process Institutional Review Board submissions and other regulatory submissions, including initial submissions, amendments, continuing reviews, adverse events, and serious adverse events.
  • Coordinate, organize, and maintain documentation required by sponsors or contract research organizations, including case report forms, source documentation, study and regulatory binders, and subject binders.
  • Assist in coordinating Phase I through Phase IV clinical trials.
  • Participate in study audits conducted by sponsors, contract research organizations, the Food and Drug Administration, and other entities as required.
  • Schedule patient visits and necessary testing.
  • Process and ship blood, urine, and tissue samples as required by trials.
  • Conduct initiation, monitoring, and closeout visits with sponsors or contract research organizations.
  • Ensure screening and enrollment of study participants, including administering informed consent and confirming eligibility before participation.
  • Report serious and non-serious adverse events to sponsors and applicable institutional or study-related committees and personnel according to regulations and policies.
  • Coordinate administration of investigational products and study-related medications, including obtaining orders, scheduling administration dates, administering medications as applicable, and monitoring subjects for post-administration adverse events or reactions.
  • Manage scheduling and coordination of study-specified treatments, follow-up visits, and procedures.
  • Meet routinely with the Principal Investigator to discuss study-related issues and ensure completion of study-related procedures.
  • Collect data from source documents for study visits and transcribe it to case report forms, including concomitant medications and adverse events.
  • Prepare study-related document templates, subject study binders, regulatory binders, and patient enrollment logs for study start-up.
  • Prepare required study-related documents for submission to applicable University of Pennsylvania institutional committees for review and approval to start trials.
  • Assist with protocol development to ensure logistical feasibility of study procedures and workflow.
  • Manage multiple clinical trials and responsibilities within a specific research area.
  • Coordinate patient screening, subject enrollment, biological sample collection and storage, clinical data collection, Institutional Review Board filings and inquiries, and preparation of manuscripts, grant proposals, and research presentations.
  • Work with the Principal Investigator, manager, and study team to identify problems and develop solutions.
  • Implement approved procedural changes and monitor results.
  • Coordinate investigator-initiated studies, multicenter research studies, and patient-oriented clinical and translational research projects.
  • Facilitate, promote, and ensure good clinical practice in research protocols.
  • Independently manage phases of complex clinical trials and mentor coordinators and research assistants.
  • Work with partnering institutions, create multicenter budgets, and manage expenses.
  • Participate in study team, disease site group, protocol training, and compliance meetings.
  • Support monitoring of external sites and management of multisite trials.
University of Pennsylvania

University of Pennsylvania

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The University of Pennsylvania is a private Ivy League research university in Philadelphia. It comprises twelve undergraduate, graduate, and professional schools, including the Wharton School, Perelman School of Medicine, and Penn Carey Law.

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