Not specified; not specified; competitive benefits...
On-site
Good clinical practice (gcp) compliance
Protocol adherence and execution
Site initiation and closure visits
Bristol Myers Squibb is seeking a Clinical Trial Monitor responsible for overseeing clinical trial progress and ensuring compliance with protocols and regulations. The ideal candidate will have relevant clinical research experience and a strong ability to manage site relationships and monitor trial activities
Job Summary
The role is responsible for overseeing clinical trial progress to ensure compliance with protocols, SOPs, and GCP guidelines.
Employees will act as a key point of contact for sites, conducting initiation visits, monitoring activities, and resolving issues proactively.
Bristol Myers Squibb offers a flexible work environment with competitive benefits and opportunities to transform patients' lives through science.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Clinical Trial Monitor responsible for overseeing clinical trial progress and ensuring compliance with protocols and regulations. The ideal candidate will have relevant clinical research experience and a strong ability to manage site relationships and monitor trial activities.
Salary
Not specified; Not specified; Competitive benefits and programs provided
Skills & Requirements
Must-have
Good Clinical Practice (GCP) compliance
Protocol adherence and execution
Site initiation and closure visits
Data quality assurance and eCRF review
Risk-based monitoring activities
Nice-to-have
Leadership and mentoring capabilities
Cross-therapeutic area experience
Strong stakeholder communication skills
Adaptability in diverse work environments
Key Requirements
Bachelor's or Master's degree in life sciences
2-3 years of clinical research monitoring experience
Experience with drug discovery/development process