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.