Work Set‑Up: On‑site
Schedule: Part‑time | 24 hours per week
About IQVIA
IQVIA is a global leader in advanced analytics, technology solutions, and clinical research services, dedicated to driving healthcare forward. We partner with leading pharmaceutical, biotechnology, and medical device organizations to improve patient outcomes and accelerate innovation. Our teams combine scientific expertise with cutting‑edge technology to deliver high‑quality clinical research that advances medicine.
About the Role
IQVIA is seeking a Clinical Research Coordinator (CRC) to support the execution of clinical research studies conducted under the supervision of a Principal Investigator. This role is ideal for a detail‑oriented, patient‑focused professional who thrives in a hands‑on clinical setting and is experienced in study coordination, patient visits, and data quality.
Key Responsibilities
Perform clinical research procedures, including ECGs, vital signs, and biological sample collection
Coordinate day‑to‑day clinical research activities in accordance with study protocols and GCP requirements
Prepare study materials, set up equipment, and support logistical planning for research visits
Recruit, screen, prescreen, and orient study participants while ensuring patient safety and protocol adherence
Lead and conduct subject study visits in alignment with protocol and investigator oversight
Accurately collect, review, and document clinical data in case report forms (CRFs) and EDC systems
Collaborate with investigators, study monitors, and site staff to resolve queries and maintain data integrity
Serve as a patient advocate and maintain a safe clinical environment consistent with Health & Safety policies
Qualifications
Bachelor’s degree preferred or an equivalent combination of education and relevant experience
Minimum of 1+ years of clinical research experience
Ability to conduct patient chart review and prescreen subjects against inclusion/exclusion criteria
Experience independently leading subject study visits
Prior experience with EDC data entry and query resolution
Working knowledge of clinical trial conduct, GCP principles, and medical terminology
Strong attention to detail with the ability to establish effective working relationships
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.