Bristol Myers Squibb is seeking a Clinical Trial Monitor responsible for overseeing clinical trial progress, ensuring compliance with protocols and regulations, and developing site relationships. The role requires experience in clinical research, with a focus on collaboration and effective communication with various stakeholders
Job Summary
The role involves overseeing clinical trials to ensure they are conducted in accordance with protocols, SOPs, and GCP guidelines.
Employees will act as a key point of contact for sites, managing relationships and ensuring safety and protection of study subjects.
Bristol Myers Squibb offers a wide variety of competitive benefits and programs to support employee goals both at work and in personal lives.
Matching Summary
Match Score: 85
Bristol Myers Squibb is seeking a Clinical Trial Monitor responsible for overseeing clinical trial progress, ensuring compliance with protocols and regulations, and developing site relationships. The role requires experience in clinical research, with a focus on collaboration and effective communication with various stakeholders.
Skills & Requirements
Must-have
Good Clinical Practice (GCP) compliance
protocol adherence and monitoring
site initiation and closure visits
data integrity and eCRF review
risk-based monitoring approach
Nice-to-have
mentoring and coaching capabilities
cross-therapeutic area experience
strong stakeholder communication skills
proactive issue resolution mindset
Key Requirements
Bachelor's or Master's degree in life sciences
1-5 years of relevant clinical research experience depending on level
Experience in drug discovery/development process preferred