Bristol Myers Squibb in the United Kingdom seeks a Regulatory Documentation Specialist to lead authoring of regulatory documents for submissions and approvals in key markets, coordinating input from scientific, medical, and regulatory teams to ensure timely, high-quality outputs.
The role requires a BS/BA in science with 1–2 years of regulatory writing or related experience; PhD/PharmD candidates are welcome. Strong writing, planning, and cross-functional collaboration are essential.
#J-18808-LjbffrPatient Safety Regulatory Writing Manager in Uxbridge 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.
