Clinical Research Coordinator - Philadelphia, PA

divh2Clinical Research Coordinator - Philadelphia, PA/h2pPhiladelphia, United States of America | Part time | Office-based | R1544815/ppClinical Research Coordinator Philadelphia, PA/ppWork Setup: On-site Employment Type: Part-time - 24 Hours per Week/ppIQVIA 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./ppPosition Overview/ppWe 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./ppKey Responsibilities/pulliPerform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols/liliCoordinate day-to-day clinical trial activities while ensuring compliance with GCP, protocol, and regulatory requirements/liliPrepare study materials, organize equipment, and support overall site readiness/liliConduct patient recruitment activities, including chart review, phone screening, and scheduling study visits/liliPerform and manage patient study visits in accordance with protocol requirements/liliEducate and orient participants, ensuring a high standard of patient care and safety/liliAccurately collect, document, and enter data into EDC systems and case report forms (CRFs)/liliResolve data queries in a timely manner and maintain high data quality standards/liliCollaborate with investigators, sponsors, and monitors during site visits and audits/liliServe as a patient advocate and maintain a safe, compliant clinical environment/li/ulpQualifications/pulliBachelors degree preferred, or an equivalent combination of education and relevant experience/liliMinimum of 1+ years of clinical research experience in a coordinator or similar role/liliWorking knowledge of clinical trial processes, GCP guidelines, and medical terminology/liliProven ability to conduct patient study visits in accordance with protocol requirements/liliExperience in patient recruitment, including chart review and phone screenings/liliProficiency with EDC systems, including accurate data entry and query resolution/liliStrong attention to detail, organizational skills, and ability to manage multiple priorities/liliEffective communication skills and ability to build collaborative working relationships/liliCardiovascular research experience preferred/li/ulpWhy Join IQVIA?/pulliBe part of a global organization at the forefront of clinical innovation/liliCollaborate with industry-leading experts and researchers/liliContribute to advancing treatments that improve patient lives/li/ulpNote: This position is not eligible for visa sponsorship/pp#LI-CES and #LI-DNP #LI-HCP #remote/ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism./p/div