Clinical Research Coordinator - New York, NY
IQVIA•Parsippany, NJ
•Onsite
About The Position
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.
Requirements
- 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
Nice To Haves
- Experience in Neurology and/or Pediatrics is a plus, but not required
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
Benefits
- health and welfare and/or other benefits
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What This Job Offers
Job Type
Part-time
Career Level
Mid Level
