About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with the world’s leading pharmaceutical, biotechnology, and medical device companies to improve patient outcomes and accelerate innovation. Our teams combine deep scientific expertise with cutting‑edge technology to deliver high‑quality data and insights that shape the future of clinical trials.
About the Role
IQVIA is seeking a Clinical Research Coordinator (CRC) to support clinical research studies conducted under the supervision of a Principal Investigator. This role is hands‑on and patient‑focused, requiring experience in clinical procedures, patient recruitment, and accurate data collection while ensuring compliance with study protocols and regulatory standards.
Key Responsibilities
Perform clinical research procedures, including ECGs, vital signs, and biological sample collection
Coordinate clinical research studies in compliance with study protocols and Good Clinical Practice (GCP) guidelines
Prepare study materials, set up equipment, and support logistical planning for research activities
Recruit, screen, prescreen, and orient study participants, ensuring patient safety and protocol adherence
Collect, review, and accurately document clinical data in case report forms (CRFs) and electronic systems
Collaborate with investigators and study monitors to address data queries and maintain data quality
Act as a patient advocate and maintain a safe clinical environment in accordance with Health & Safety policies
Qualifications
Bachelor’s degree preferred or an equivalent combination of education and relevant experience
Minimum of 1+ years of relevant clinical research experience
Working knowledge of clinical trials, GCP principles, and medical terminology
Strong attention to detail with the ability to establish effective working relationships
Proficiency with EDC systems, including accurate data entry and query management
Experience with cardiovascular research or cardiovascular patient populations
Ability to conduct patient chart review and pre‑screening against inclusion/exclusion criteria
Experience using NextGen EMR, including clinical documentation and data entry
Note: This position is not eligible for sponsorship
#LI-CES and #LI-DNP #LI-HCP #remote
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.