Clinical Research Coordinator – Philadelphia, PA

Work Setup: On-site
Employment Type: Full-time

About IQVIA

IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. By combining deep scientific expertise with cutting-edge technology, we deliver high-quality data and insights that shape the future of clinical trials.

Position Overview

We are seeking a Clinical Research Coordinator (CRC) to support the successful execution of clinical research studies under the direction of a Principal Investigator. This is a hands-on role requiring clinical, operational, and patient-facing expertise to ensure studies are conducted safely, efficiently, and in compliance with regulatory standards.

Key Responsibilities

• Perform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols

• Coordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements

• Prepare study materials, organize equipment, and support overall site readiness

• Conduct patient recruitment activities, including chart review, phone screening, and scheduling study visits

• Perform and manage patient study visits in accordance with protocol requirements

• Educate and orient participants, ensuring a high standard of patient care and safety

• Accurately collect, document, and enter data into EDC systems and case report forms (CRFs)

• Resolve data queries in a timely manner and maintain high data quality standards

• Collaborate with investigators, sponsors, and monitors during site visits and audits

• Serve as a patient advocate and maintain a safe, compliant clinical environment

Qualifications

• Bachelor’s degree preferred, or an equivalent combination of education and relevant experience

• Minimum of 1+ years of clinical research experience in a coordinator or similar role

• Working knowledge of clinical trial processes, GCP guidelines, and medical terminology

• Proven ability to conduct patient study visits in accordance with protocol requirements

• Experience in patient recruitment, including chart review and phone screenings

• Proficiency with EDC systems, including accurate data entry and query resolution

• Strong attention to detail, organizational skills, and ability to manage multiple priorities

• Effective communication skills and ability to build collaborative working relationships

• Cardiovascular research experience preferred

Why Join IQVIA?

• Be part of a global organization at the forefront of clinical innovation

• Collaborate with industry-leading experts and researchers

• Contribute to advancing treatments that improve patient lives

Note: This position is not eligible for visa sponsorship