Clinical Trial Monitor

Bristol Myers Squibb

Multiple Locations
Gcp and regulatory requirements
Protocol and sop adherence
Site relationship management
Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s)

Job Summary

  • Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s).
  • Manages multiple protocols, across multiple therapeutic areas, which may require travel, based upon assigned site location and/or geographic territory.
  • BMS is dedicated to ensuring that people with disabilities can excel through a transparent recruitment process, reasonable workplace accommodations/adjustments and ongoing support in their roles.

Matching Summary

Responsible for the oversight of the progress of a clinical trial, and of ensuring that it is conducted, recorded, and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the applicable regulatory requirement(s).

Skills & Requirements

Must-have

  • GCP and regulatory requirements
  • protocol and SOP adherence
  • site relationship management
  • risk assessment and issue resolution
  • data quality oversight

Nice-to-have

  • patient safety and protection
  • diversity in clinical trials
  • adaptability and flexibility
  • proactive problem solving

Key Requirements

  • Bachelors or Masters degree
  • 1-5 years clinical research experience
  • Pharma/Biotech Sponsor employment preferred
  • Drug discovery/development process experience

Work Rights

Not specified

Tailored Resume

Cover Letter