$71,900 – $182,000
Listed on IQVIA’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
IQVIA is seeking a Clinical Research Associate to oversee oncology trial sites, managing monitoring visits, regulatory compliance, and data integrity across US locations. This role suits candidates with 1-2 years of clinical research monitoring experience who can coordinate between study teams and research sites to ensure protocol adherence and timely enrollment.
Our summary, not IQVIA’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's degree in scientific or health care discipline, or equivalent combination of education and experience
- 1-2 years of onsite monitoring experience
- Knowledge of GCP and ICH regulatory requirements
- Proficiency with Microsoft Office applications and laptop/mobile devices
- Written and verbal communication skills in English
- Ability to travel for site monitoring visits
Nice to have
- Experience in Cardiovascular, Renal, Metabolic, Oncology, or Neurology therapeutic areas
- Completion of CRA training program
- Prior clinical research monitoring experience