Clinical Research Coordinator - Philadelphia, PA

IQVIA•Parsippany, PA

1d•Onsite

About The Position

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. 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.

Requirements

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

Nice To Haves

Cardiovascular research experience preferred

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