# Clinical Trial Monitor

Hiring organization: [Bristol Myers Squibb](https://career.thegoodapps.co/organizations/bristol-myers-squibb)

Canonical page: https://career.thegoodapps.co/jobs/a5f35a1f-2e4c-4f09-a6dd-61bf7652efa0

Listed on Bristol Myers Squibb's own careers site. Applications go to them directly.

- Seniority: Mid

## Summary

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._

## Skills named

Good Clinical Practice, Regulatory Compliance

## 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

Apply on Bristol Myers Squibb's site: https://bristolmyerssquibb.wd5.myworkdayjobs.com/en-US/BMS/job/Shanghai---CN/Clinical-Trial-Monitor_R1564460