Clinical Research Coordinator - Abington, PA

divh2Clinical Research Coordinator - Abington, PA Work Set?Up: On?site Scheduled Weekly Hours: 24 hours per week/h2pIQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with the worlds 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./ph3About the Role/h3pIQVIA 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./ph3Key Responsibilities/h3ulliPerform clinical procedures such as ECGs, vital signs, and biological sample collection in accordance with study protocols./liliCoordinate daily clinical research activities while ensuring compliance with study requirements, Good Clinical Practice (GCP), and regulatory standards./liliPrepare, organize, and maintain study materials, equipment, and documentation to support study conduct./liliRecruit, screen, consent, and orient study participants, ensuring a positive and safe patient experience throughout the trial lifecycle./liliConduct study visits, including informed consent, participant education, collection of medical history and medication information, and follow?up activities./liliAccurately collect, document, and enter clinical data into case report forms (CRFs) and electronic data capture (EDC) systems./liliCollaborate with investigators, monitors, and study team members to resolve data queries and maintain high data quality./liliServe as a patient advocate while maintaining a safe clinical environment in alignment with Health and Safety policies./li/ulh3Qualifications/h3ulliBachelors degree preferred, or an equivalent combination of education and relevant clinical research or healthcare experience./liliMinimum of 1+ year of clinical research experience, including hands?on study coordination responsibilities./liliExperience coordinating clinical research studies and supporting protocol execution from participant recruitment through study visits./liliComfortable independently conducting study visits, including informed consent, vital signs collection, medical history review, and documentation of medications./liliWorking knowledge of clinical trials, GCP principles, and medical terminology./liliExperience with EDC systems, including accurate data entry and data query resolution./liliFamiliarity with regulatory binders, study supply management, and study portals./liliStrong attention to detail with the ability to build effective working relationships across clinical and research teams./li/ulpPlease note: This position is not eligible for sponsorship./p/div