Clinical Trial Monitor
Bristol-Myers Squibb- Knowledge of clinical trial protocols, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), ICH/GCP Guidelines, and applicable regulatory requirements - Ability to assess risks using data, identify issues, and make appropriate decisions - Ability to manage multiple protocols across multiple therapeutic areas - Willingness to travel based on assigned site location and/or geographic territory - Flexibility and adaptability in communication with different stakeholders - Skills in r…
Salary not specified
Full Time
Mid-level (3 to 4 years)