Bristol Myers Squibb UK is seeking a Regulatory Writing professional to lead authoring of message-driven regulatory documents for submissions and lifecycle management within the BMS pipeline.
You will coordinate cross-functional input, ensure timely production of documents (IBs, CSR, RMPs, protocols) and maintain document prototypes while complying with internal and external guidelines. On-site/hybrid roles with flexible work arrangements.
#J-18808-LjbffrSenior Patient Safety Regulatory Writer in Uxbridge employer: Bristol Myers Squibb EU Policy
At Bristol Myers Squibb, we offer a unique opportunity to engage in challenging and meaningful work that truly transforms lives. Our collaborative culture fosters inclusiveness and respect for diversity, while providing exceptional growth opportunities through mentorship and innovative projects in the pharmaceutical industry. Join us in a dynamic environment where your contributions will not only advance your career but also make a significant impact on patient outcomes.
Contact Details:
Bristol Myers Squibb EU Policy Recruitment Team
