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Senior Regulatory Affairs Manager - CMC bio/vax (various European locations - home or office based)

Parexel

United Kingdom-Harrow-RemotePosted 18 h agoRemoteDirect from company

  • LocationUnited Kingdom-Harrow-Remote; United Kingdom-London-Gridiron; Croatia-Remote; Hungary-Budapest +6 more
  • Work typeRemote
  • EmploymentFull-time
  • Posted3 November 2026
  • SourceParexel's careers page (Workday)
  • Last checked6 h ago on Parexel's careers page
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About the role

When our values align, there's no limit to what we can achieve.

At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.
Each of us, no matter what we do at Parexel, contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference.

We are looking for a Senior Regulatory Affairs Manager/Consultant with 10+ years of experience in regulatory affairs, including CMC expertise. This challenging role offers the opportunity to work on diverse projects, manage client relationships, and contribute to regulatory strategies in a global pharmaceutical environment.

This is a client dedicated project, without people management responsibility. The role can be home or office based in various European locations.

Key Responsibilities:

- Write CMC sections and scientific rationales for regulatory submissions and responses

- Develop and implement variations strategies based on EU guidelines

- Coordinate CMC activities across multiple projects

- Liaise with global affiliates and manufacturing sites

- Provide project leadership and management

- Ensure client satisfaction and project quality

- Identify new business opportunities and contribute to proposal preparation

Required Qualifications:

- 10+ years of experience in regulatory affairs

- Extensive knowledge of CMC writing and variations strategy

- Working knowledge of vaccines or biological processes - required

- Experience with regulatory agencies (e.g., FDA, EMA, MHRA)

- In-depth understanding of EU guidelines (Variation, ICH, EMA)

- Excellent project management and organizational skills

- Strong communication abilities and client management experience

- Ability to work independently and as part of a team

- Fluent in English written and spoken; additional languages are a plus

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