HealthcareOn site
Sr. CRA, Oncology, IQVIA Biotech
IQVIADurham, NC
$105,100–197,500/yr
Posted Sep 29, 2026
What you’d do
Independently manage and monitor clinical trial sites for biotech sponsors, ensuring compliance with study protocols, GCP, ICH guidelines, and FDA regulations. Full-time role on the Clinical Monitoring team. Found on the employer's careers page on Oct 18, 2026. Apply through the link.
You’ll need
- Bachelor's in scientific, healthcare, or related discipline
- 4+ years on-site clinical monitoring experience
- Knowledge of GCP and ICH guidelines
- Knowledge of FDA regulations
- Clinical trial process experience
Our summary of the listing. The full listing has the details.