Regeneron UK Limited Posted October 28, 2026

Associate Director, Global Patient Safety Sciences

Uxbridge1, United Kingdom Full time
Regulatory Affairs Associate Director
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Regeneron UK Limited is the source of truth for this posting and owns the application process. We surface normalized context and market comparison you won't find on the original listing.

About this opportunity

Build our future together:

At Regeneron, we use science and innovation to develop life-changing medicines for people with serious diseases. We are seeking an Associate Director, Global Patient Safety Sciences to join our Global Patient Safety function, supporting clinical development and post-marketing activities in a hybrid work mode. In this role, you will lead safety surveillance, signal evaluation and benefit-risk assessments while collaborating with clinical study teams and cross-functional safety committees. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

Multiple locations are being considered for this role (Hybrid)

Discover your role:

Complete signal detection activities aligned with approved safety surveillance plans.

Evaluate identified signals and author safety evaluation reports.

Manage safety documents, including DSURs, PSURs, RMPs and health authority responses.

Present at Signal Management Team meetings and support assigned clinical study teams.

Represent GPS on cross-functional safety committees and external Independent Data Monitoring Committees.

You will strengthen safety processes by maintaining SOPs, working instructions and supporting documents.

This role requires:

Master’s degree, PhD or PharmD.

At least 10 years’ relevant pharmaceutical, biotechnology or health authority experience.

Risk management, pharmaceutical safety or relevant clinical experience.

Knowledge of FDA, EU and ICH pharmacovigilance requirements.

Experience using safety databases for medical case review and simple queries.

Clear safety communication, prioritisation, self-discipline and proactive delivery.

Therapeutic-area clinical or industry experience is advantageous.

Board certification is preferred.

Does this sound like you? Apply now to take your first step towards living the Regeneron Way! We are committed to building a workplace with an inclusive culture. Regeneron is an equal opportunity employer and all  qualified applicants will receive consideration for employment without regard to race, color, religion or belief (or lack thereof), sex, sexual orientation, gender identity or expression, gender reassignment, marital or civil partnership status, civil status, pregnancy or parental status, age, disability, nationality, citizenship status, ethnic or national origin, membership of the Traveler community, familial status, genetic information, military or veteran status, or any other characteristic protected under applicable law. Where required, we will provide reasonable accommodation to applicants with known disabilities or chronic illnesses during the recruitment process, unless such accommodation would impose undue hardship.

Where necessary, we disclose salary ranges for roles in all countries in which we operate.  The final offer will be determined within the relevant range based on the country of employment, specific role level, and your skills and experience. In some countries, collective bargaining agreements (CBAs) may apply and influence certain elements of pay or benefits.  Regeneron offers a competitive and comprehensive total rewards package which may include, depending on country and role: annual bonuses or other incentive plans, equity awards, pension or retirement benefits, 401(k) company match, health and wellness programs, fitness centers, insurance benefits (e.g. medical, dental, vision, life and disability), paid time off, and family support benefits. For additional information about Regeneron benefits in the U.S., please visit https://careers.regeneron.com/en/working-at-regeneron/total-rewards/ . For other locations, additional information will be provided during the recruitment process.  If you have any questions, please speak with your recruiter.

Please be advised that at Regeneron, we believe we do our best work when we are together. For that reason, many roles are required to be performed on‑site. Please speak with your recruiter and hiring manager for more information about on‑site expectations for your role and location.

As part of the recruitment process, certain background checks may be conducted in accordance with the laws of the country where the position is based. The purpose of such checks is to verify certain information prior to the commencement of employment such as identity, right to work and educational qualifications.

For jobs in Canada: this posting is for an existing position.

Job details

Seniority
Associate Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Uxbridge1, United Kingdom
Employment type
Full time

How this role compares

Computed from every other active Regulatory Affairs role in our database, not just this employer's listings.

We currently track 290 comparable Associate Director Regulatory Affairs roles across 79 biopharma companies.

290Comparable roles tracked
264Currently active
79Companies hiring similar roles
38Countries represented

Salary context

82 of 290 peers report a salary range (USD, annualized)

Peers share this role's job function and a matching or adjacent seniority level -- not necessarily the same therapeutic area or country.

This roleSubject Not listed on this posting
Lowest disclosed · Senior Regulatory Affairs Specialist · Johnson & Johnson $92,000/yr – $148,350/yr
Peer group range $120,175 – $236,300 (median $180,500)

Where these roles are based

Top locations among the 290 comparable roles

United States118
India26
United Kingdom20
Japan18
Ireland14
Poland14

+ 32 more countries

Seniority mix

290 of 290 peers have a known seniority level

Manager178
Associate Director56
Senior56

Therapeutic area mix

27 of 290 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology13
Oncology7
Dermatology & Aesthetics5
Vaccines & Infectious Disease1
Respiratory1

Similar opportunities

The closest matches from our peer group, ranked by how similar they are, not how well you'd qualify for them -- treat this as market context, not a guaranteed shortlist; a weak match is labeled as one below.

60%similar
Regeneron UK Limited Uxbridge1, United Kingdom Associate Director
Same function Same seniority Same country
50%similar
AbbVie Marlow, England Manager
Same function Adjacent seniority Same country
50%similar
Amgen Limited Uxbridge, United Kingdom Manager
Same function Adjacent seniority Same country
50%similar
Perrigo London, United Kingdom Senior
Same function Adjacent seniority Same country
50%similar
Perrigo London, United Kingdom Senior
Same function Adjacent seniority Same country
50%similar
Ipsen Biopharm Ltd London (UK), United Kingdom Manager
Same function Adjacent seniority Same country

Notify me about similar jobs

Get an email when we spot other openings like this one – same job function, comparable seniority, roles you'd actually want to see.

Or follow a whole field: get every new Regulatory Affairs job in the United Kingdom, and choose locations and companies.

How we calculate "similar"

No black box, no LLM guesswork: a deterministic score built from four normalized attributes. Here's this role's own peer group at different match levels, so you can see the mechanism, not just the result.

Every comparison starts from the same 100-point budget: 25 for working in the same function, 40 for the same therapeutic area, 20 for the same or adjacent seniority, 15 for the same country. A dimension we can't confirm on both sides contributes nothing, never a guess, never a free pass.

60%
Associate Director, Global Patient Safety Standards & Training
Regeneron UK Limited · Uxbridge1, United Kingdom · Associate Director
Function Therapeutic area Seniority Country
50%
EU Regulatory Affairs Manager (Biosimilars)
Amgen Limited · Uxbridge, United Kingdom · Manager
Function Therapeutic area Adjacent seniority Country
50%
Regulatory Submission Project Manager
Ipsen Biopharm Ltd · London (UK), United Kingdom · Manager
Function Therapeutic area Adjacent seniority Country
50%
EU Regulatory Affairs Manager
Amgen Limited · Uxbridge, United Kingdom · Manager
Function Therapeutic area Adjacent seniority Country
Unmatched or unknown dimensions score exactly the same: 0 points, never a partial guess. A role we know almost nothing about beyond its function bottoms out at 25%; it never inflates to 100% just because there's little to compare against. Seniority uses a defined ladder (Associate → Manager → Associate Director → Senior → Principal → Director → Senior Director → Executive/VP) so "Director" and "Senior Director" count as adjacent, but "Director" and "Executive/VP" do not.