53476Posted: 21/09/2026London, United Kingdom Permanent I'm supporting a UK-based clinical-stage biotechnology company with the appointment of a Senior Manager, Regulatory Affairs. This is a senior, hands-on regulatory role supporting a development programme as it progresses into late-phase clinical development. The position will play a key role in shaping and executing global regulatory strategy across major markets, including the FDA, EMA, MHRA, Health Canada and TGA, while working closely with senior internal stakeholders and external regulatory partners. Supporting global regulatory and development strategy Managing regulatory planning, commitments and key milestones Overseeing CROs, consultants and external regulatory service providers Supporting regulatory and inspection readiness Developing and improving regulatory processes, SOPs and governance Providing regulatory input into cross-functional development plans and key programme decisions Supporting and managing members of the Regulatory Affairs team Significant Regulatory Affairs experience within pharma or biotech Hands-on experience with regulatory submissions and health authority interactions Strong regulatory operations and project management capability Experience working within an outsourced or virtual biotech model
Senior Regulatory Affairs Manager Contract in London employer: Barrington James
Barrington James is an exceptional employer that fosters a collaborative and innovative work culture, making it an ideal place for professionals in Epidemiology and Real-World Evidence. With a strong emphasis on employee growth, we offer tailored development opportunities and the chance to lead impactful projects across diverse therapeutic areas in the dynamic UK/Europe market. Join us to be part of a team that values flexibility, creativity, and meaningful contributions to healthcare advancements.
