About IQVIA
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
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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 https://jobs.iqvia.com
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. https://jobs.iqvia.com/eoe
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.
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.