Clinical Research Coordinator - Abington, PA
Work Set‑Up: On‑site
Scheduled Weekly Hours: 24 hours per week

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to drive healthcare innovation. By combining deep scientific expertise with cutting‑edge technology, we deliver high‑quality data and insights that accelerate development and improve patient outcomes worldwide.

About the Role

IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies under the supervision of a Principal Investigator. This role is essential to the successful execution of clinical trials and involves a mix of study coordination, hands‑on clinical procedures, and direct participant interaction. The ideal candidate is detail‑oriented, organized, and comfortable managing study visits while ensuring compliance, data integrity, and participant safety.

Key Responsibilities

• Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols.
• Coordinate daily clinical research activities while ensuring compliance with study requirements, Good Clinical Practice (GCP), and regulatory standards.
• Prepare, organize, and maintain study materials, equipment, and documentation to support study conduct.
• Recruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial lifecycle.
• Conduct study visits, including informed consent, participant education, collection of medical history and medication information, and follow‑up activities.
• Accurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems.
• Collaborate with investigators, monitors, and study team members to resolve data queries and maintain high data quality.
• Serve as a patient advocate while maintaining a safe clinical environment in alignment with Health and Safety policies.

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant clinical research or healthcare experience.
• Minimum of 1+ year of clinical research experience, including hands‑on study coordination responsibilities.
• Experience coordinating clinical research studies and supporting protocol execution from participant recruitment through study visits.
• Comfortable independently conducting study visits, including informed consent, vital signs collection, medical history review, and documentation of medications.
• Working knowledge of clinical trials, GCP principles, and medical terminology.
• Experience with EDC systems, including accurate data entry and data query resolution.
• Familiarity with regulatory binders, study supply management, and study portals.
• Strong attention to detail with the ability to build effective working relationships across clinical and research teams.