Job Description

Position Title: Clinical Research Coordinator

Location: Philadelphia, Pennsylvania

Summary:

The Clinical Research Coordinator is responsible for coordinating and facilitating clinical research protocols across assigned sites. This role ensures protocol compliance, participant safety, and accurate data collection, while serving as a key liaison among investigators, sponsors, healthcare teams, and participants.

Responsibilities:

• Coordinate clinical research studies, including participant recruitment, screening, informed consent, and data collection.
• Collect, process, and ship research specimens in compliance with IATA guidelines.
• Monitor participant safety, adverse events, and protocol deviations.
• Support investigators during study initiation, monitoring, and close-out visits.
• Provide education and guidance to participants, families, and clinical staff regarding study procedures.
• Assist with regulatory submissions, quality assurance activities, and study documentation.
• Maintain accurate study records, data entry, and reporting to meet sponsor and regulatory requirements.

Qualifications:

• Education: Bachelor’s degree required; advanced coursework or degree in a related field preferred.
• Experience: Minimum 1 year in a clinical research setting (oncology experience preferred).
• Certifications: CCRC, CCRP, or CCRA preferred (IATA certification required within 3 months of hire).
• Skills: Strong organizational and communication skills; proficiency with Microsoft Office; knowledge of medical terminology; ability to manage multiple studies and deadlines.

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