Clinical Research Coordinator — Flexible Hours & Phase Trials

University of Pennsylvania Perelman School of Medicine; Philadelphia (Philadelphia County); On-site; USD 57,000 - 69,000; Full time

Benefits offered by this job

Tuition benefits

Excellent healthcare

Professional development

Job summary

The University of Pennsylvania Perelman School of Medicine is seeking a Clinical Research Coordinator C to support Phase I–IV clinical trials. You will coordinate visits, collect samples, and ensure protocol adherence, while maintaining regulatory compliance with IRB, sponsors, and CROs.

Required qualifications include a Bachelor of Science and 4–6 years of experience, plus strong communication skills and knowledge of CFR/ICH/GCP guidelines.

Qualifications

• Bachelor of Science and 4–6 years of experience coordinating day-to-day activities of multiple therapeutic research protocols.
• Strong verbal and written communication skills; ability to multi-task and work in a team or independently.
• Working knowledge of CFR, ICH, and GCP guidelines; ability to learn new methods quickly.

Responsibilities

• Coordinate the conduct of Phase I–IV clinical trials.
• Prepare and process regulatory documentation and submissions to IRB, sponsors, and CROs.
• Organize source documents, case report forms, study and regulatory binders, and ensure data quality.

Skills

Verbal and written communication

Teamwork

Flexibility

Attention to detail

Education

Bachelor of Science

Tools

EMR system

Regulatory documentation tools

Job description

The University of Pennsylvania Perelman School of Medicine is seeking a Clinical Research Coordinator C to support Phase I–IV clinical trials. You will coordinate visits, collect samples, and ensure protocol adherence, while maintaining regulatory compliance with IRB, sponsors, and CROs.

Required qualifications include a Bachelor of Science and 4–6 years of experience, plus strong communication skills and knowledge of CFR/ICH/GCP guidelines.