What are the responsibilities and job description for the Executive Director of Clinical Operations position at Bristol-Myers Squibb?
About Us
Bristol Myers Squibb is a global biopharmaceutical company that has been transforming patients' lives through science for over 125 years. Our mission is to deliver innovative medicines and solutions that help patients overcome life-threatening diseases. We are committed to advancing the field of healthcare and improving the quality of life for patients around the world.
Job Description
The Regional Head of Clinical Operations will provide strategic leadership and direction to clinical trial teams in the United States and Canada. This role will be responsible for developing and implementing strategies to ensure successful execution of clinical trials, as well as providing guidance and support to site staff. The ideal candidate will have a strong background in clinical operations, excellent leadership skills, and the ability to work effectively in a fast-paced environment.
Key Responsibilities
Bristol Myers Squibb is a global biopharmaceutical company that has been transforming patients' lives through science for over 125 years. Our mission is to deliver innovative medicines and solutions that help patients overcome life-threatening diseases. We are committed to advancing the field of healthcare and improving the quality of life for patients around the world.
Job Description
The Regional Head of Clinical Operations will provide strategic leadership and direction to clinical trial teams in the United States and Canada. This role will be responsible for developing and implementing strategies to ensure successful execution of clinical trials, as well as providing guidance and support to site staff. The ideal candidate will have a strong background in clinical operations, excellent leadership skills, and the ability to work effectively in a fast-paced environment.
Key Responsibilities
- Develop and implement strategic plans to ensure successful execution of clinical trials.
- Provide guidance and support to site staff to ensure compliance with regulatory requirements.
- Collaborate with cross-functional teams to develop and implement clinical trial protocols.
- Maintain accurate records and reports to track clinical trial progress.
- Identify and mitigate risks associated with clinical trial execution.
