Listed on Bristol Myers Squibb’s own careers site. You apply with them directly — we never stand between you and the employer.
What this role is
Bristol Myers Squibb is seeking a Clinical Trial Monitor to oversee the conduct, documentation, and regulatory compliance of clinical trials across multiple sites and therapeutic areas. This role suits healthcare professionals with clinical research experience who are comfortable with independent site management, regulatory oversight, and travel-based work.
Our summary, not Bristol Myers Squibb’s wording. The full posting is on their site.
Skills this role names
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What they ask for
Required
- Bachelor's or Master's degree in life sciences or equivalent
- 2–3 years of relevant clinical research experience
- Ability to work independently
- Conduct site monitoring visits and assessments
- Ensure protocol compliance and data quality
- Manage multiple protocols across therapeutic areas
- Travel to assigned sites as needed
Nice to have
- Prior pharma or biotech sponsor employment
- Experience as a clinical study coordinator
- Knowledge of drug discovery and development process
- Unblinded site monitoring experience