Bristol Myers Squibb in the United Kingdom seeks a detail-oriented Regulatory Writing professional to lead the authoring of pivotal regulatory documents across clinical pharmacology, safety and global submissions.
You will coordinate cross-functional input, ensure clear messaging, maintain document prototypes, and drive timelines to support speedy approvals and lifecycle management within the BMS pipeline. This role requires scientific rigor, strong writing skills and proficiency with MS Office.
#J-18808-LjbffrPatient Safety Regulatory Writing Lead in Denham employer: Bristol Myers Squibb
Bristol-Myers Squibb in Uxbridge is an exceptional employer, offering a dynamic work culture that prioritises collaboration and innovation. Employees benefit from extensive career growth opportunities, mentorship programs, and the chance to contribute meaningfully to life-changing clinical trials, all while enjoying a supportive environment that values data integrity and compliance.
