At IQVIA Biotech, we partner with visionary biotech companies to transform innovation into patient impact. With dedicated teams, deep therapeutic expertise, and a biotech-tailored delivery model, we accelerate clinical development from early phase through global registrational studies.
We’re seeking an experienced Clinical Research Associate with 1-3 years of onsite monitoring to oversee clinical trial sites and ensure high‑quality study execution. In this role, you’ll monitor study activity, support site teams, and ensure adherence to protocols, regulations, and sponsor expectations. Preference would be to have oncology experience but open to other therapeutic areas.
- Conduct site visits (selection, initiation, monitoring, and close‑out) in compliance with GCP, ICH, and study requirements.
- Partner with sites to drive patient recruitment and meet study enrollment goals.
- Provide study protocol and procedure training to site staff and maintain consistent communication to support study progress.
- Assess site performance, data quality, and regulatory compliance; escalate issues when needed.
- Track study milestones including submissions, approvals, enrollment, data entry, and query resolution.
- Ensure accurate and complete maintenance of site documentation and Trial Master File materials.
- Prepare monitoring reports, follow‑up letters, and other required documentation.
- Collaborate closely with the study team and provide support with start‑up activities as applicable.
- (If applicable) Support site‑level recruitment planning and financial management.
- Bachelor’s degree in a scientific or healthcare field (or equivalent experience).
- Minimum 1 year of on‑site clinical monitoring experience.
- Strong knowledge of GCP/ICH guidelines and clinical research regulatory requirements.
- Proficiency with Microsoft Office and digital tools (laptop, mobile devices).
- Excellent communication, organization, and problem‑solving skills.
- Ability to build strong working relationships with study teams, site staff, and sponsors.
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, when annualized, is $71,900.00 - $169,300.00. 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.Top Skills
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