Clinical Research Coordinator - New York, NY

Clinical Research Coordinator - New York, NY Work Set‑Up: On‑site Schedule: Part‑time | 24 hours per week IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services. We partner with leading pharmaceutical, biotechnology, and medical device organizations to accelerate clinical development and improve patient outcomes. By combining deep scientific expertise with innovative technologies, we deliver high‑quality data and insights that shape the future of healthcare. About the Role IQVIA is seeking a highly experienced Clinical Research Coordinator (CRC) to support the conduct of clinical research studies under the direction of a Principal Investigator. This role is hands‑on and patient‑facing, requiring strong clinical research expertise, the ability to manage multiple protocols, and a commitment to patient safety, regulatory compliance, and data integrity. The ideal candidate brings demonstrated experience leading study activities, coordinating visits, and supporting regulatory requirements in a fast‑paced clinical research environment. Key Responsibilities Conduct clinical research visits and procedures, including ECGs, vital signs, and biological sample collection Coordinate day‑to‑day execution of multiple clinical research protocols simultaneously Ensure strict adherence to study protocols, Good Clinical Practice (GCP), and applicable regulatory requirements Prepare study materials, organize equipment, and manage logistical planning for study visits Recruit, screen, consent, and orient study participants while ensuring safety and ethical conduct Accurately document clinical data in case report forms (CRFs) and electronic data capture (EDC) systems Collaborate with investigators, monitors, and sponsors to resolve queries and maintain data quality Provide regulatory support, including maintenance of essential documents and audit readiness Serve as a patient advocate and maintain a safe clinical environment in accordance with Health & Safety policies Required Qualifications Bachelor’s degree preferred or an equivalent combination of education and relevant experience Significant experience as a Clinical Research Coordinator, including prior responsibility as a Lead CRC managing multiple protocols concurrently Demonstrated experience conducting study visits independently and providing regulatory support Minimum of 1+ years of clinical research experience (additional experience strongly preferred) Strong working knowledge of clinical trial operations, GCP, and medical terminology Proficiency in EDC systems, data entry, and query resolution High attention to detail with the ability to build effective working relationships across cross‑functional teams Experience in Neurology and/or Pediatrics is a plus , but not required Why Join IQVIA? Be part of a globally recognized clinical research organization Work on meaningful studies that improve patient outcomes Collaborate with experienced investigators and research professionals Gain exposure to diverse protocols and therapeutic areas Note: This position is not eligible for sponsorship The potential base pay range for this role is $35.00-$42.00 per hour. The actual base pay offered may vary based on a number of factors including job‑related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part‑time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits. IQVIA 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 IQVIA 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. IQVIA 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. EEO Minorities/Females/Protected Veterans/Disabled #J-18808-Ljbffr IQVIA