Clinical Research Coordinator - Abington, PA

IQVIA • Parsippany, NJ

5d • $35 - $42 • Onsite

About The Position

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.

Requirements

• 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.
• Please note: This position is not eligible for sponsorship .

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.

What This Job Offers

• Job Type: Part-time
• Career Level: Mid Level
• Number of Employees: 5,001-10,000 employees