The role is responsible for overseeing clinical trial progress to ensure strict adherence to protocols, SOPs, and Good Clinical Practice guidelines
Job Summary
The role is responsible for overseeing clinical trial progress to ensure strict adherence to protocols, SOPs, and Good Clinical Practice guidelines.
Employees will act as a primary point of contact for sites, conducting initiation visits, monitoring activities, and resolving issues to protect study subjects.
Bristol Myers Squibb offers a flexible work environment with competitive benefits and opportunities to grow alongside high-achieving, diverse teams.
Matching Summary
The role is responsible for overseeing clinical trial progress to ensure strict adherence to protocols, SOPs, and Good Clinical Practice guidelines.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) compliance
protocol adherence and oversight
site initiation and closure visits
data review and eCRF accuracy
risk-based monitoring approach
Nice-to-have
leadership and mentoring capabilities
cross-therapeutic area experience
strong stakeholder communication skills
adaptability in diverse environments
Key Requirements
Bachelor's or Master's degree in life sciences
2-5 years of relevant clinical research experience