Associate Director, Regulatory Strategy
Alnylampharmaceuticals Is this your company? Claim it · Maidenhead · Full-time
Description
<p>The Associate Director of Regulatory Affairs Strategy will serve as an EU Regional Lead for our mid/late-stage CNS programs and may have the opportunity to be the Regulatory Program Lead for early programs in Alnylam pipeline. The will work on assigned programs with the respective Global Regulatory Portfolio Lead, Global Regulatory Lead and cross-functional team to lead the EU regulatory strategy and facilitate submission of data packages to the EMA. The role is responsible for planning and coordinating all aspects of regulatory submissions necessary to support product development, clinical trials and product registration. The role will represent RA on multidisciplinary product development subteams and Global Regulatory Team. Additional responsibilities include involvement in the writing and oversight of regulatory submissions, coordinating all aspects of paper and electronic regulatory submissions, proactively keeping updated on EU regulatory requirements, and interpreting regulatory intelligence for the internal teams.</p> <p><strong>Summary of Key Responsibilities</strong></p> <ul> <li>Serve as EU Regional Lead for assigned program (s); additional responsibilities…
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Questions about this job
Where is this Associate Director, Regulatory Strategy job located?
The listing places this job in Maidenhead.
Who is hiring?
The employer shown on the listing is Alnylampharmaceuticals.
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The listing does not state a salary. Ask the employer about pay, overtime and payment dates before accepting.
Is it full-time or part-time?
The listing type is Full-time.
When was this job posted?
It was posted on 13 November 2026. Jobs that stay open too long are closed automatically, so apply soon if you are interested.
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