Regeneron Ireland Posted November 3, 2026

Manager Regulatory Affairs

Dublin, Ireland Full time
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Regeneron Ireland 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 a Manager, Regulatory Affairs to join our regulatory function, supporting our European development programmes in a hybrid work model. In this role, you will shape EU regulatory strategy and support timely clinical development while collaborating with development teams, clinical teams, business partners, contract research organisations, and regulatory agencies. 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 position (Hybrid)

Discover your role:

Develop EU-appropriate regulatory strategies with development teams and regulatory management.

Lead clinical study submissions, agency queries, compliance, start-up, and maintenance activities.

Represent Regeneron with contract research organisations across complex late-stage clinical studies.

Support business partners in aligning EU regulatory strategy with business objectives.

Monitor emerging EU legislation and guidance, supporting company awareness and compliance.

Build relationships with the European Medicines Agency, national agencies, and alliance partners.

Lead early and late-stage regulatory strategy for timely end-to-end study conduct.

You champion innovative EU pathways and share expertise across global regulatory and development teams.

This role requires:

Advanced degree in a scientific discipline.

At least two years’ regulatory experience across clinical development and post-approval activities.

Proven experience supporting EU Clinical Trial Applications through approval and study start-up.

Direct experience with national regulatory agencies and leading face-to-face agency meetings.

Clear stakeholder negotiation and excellent written and verbal communication skills.

European Medicines Agency experience, including scientific advice, orphan designation, or paediatric investigation plans, is advantageous.

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.

Salary Range (annually)

€74,000.00 - €120,700.00

Job details

Seniority
Manager
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Dublin, Ireland
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 234 comparable Manager Regulatory Affairs roles across 73 biopharma companies.

234Comparable roles tracked
215Currently active
73Companies hiring similar roles
29Countries represented

Salary context

69 of 234 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 · Manager, Global Regulatory Strategy · Sarepta Therapeutics, Inc. $116,000/yr – $145,000/yr
Peer group range $130,500 – $236,300 (median $180,500)

Where these roles are based

Top locations among the 234 comparable roles

United States103
India26
United Kingdom20
Japan17
Ireland9
Portugal7

+ 23 more countries

Seniority mix

234 of 234 peers have a known seniority level

Manager171
Associate Director52
Associate11

Therapeutic area mix

20 of 234 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Immunology7
Oncology6
Ophthalmology4
Dermatology & Aesthetics1
Rare 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
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same seniority Same country
60%similar
Mylan Teoranta Dublin-Office, Ireland Manager
Same function Same seniority Same country
60%similar
McDermott Laboratories Limited Northern Cross, Ireland Manager
Same function Same seniority Same country
60%similar
Regeneron Ireland Dublin, Ireland Manager
Same function Same seniority Same country
60%similar
Lilly Cork, Cork, Ireland Manager
Same function Same seniority Same country
50%similar
Regeneron Ireland Dublin, Ireland Associate Director
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 Ireland, 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%
Senior Manager, Regulatory Affairs CMC
McDermott Laboratories Limited · Northern Cross, Ireland · Manager
Function Therapeutic area Seniority Country
60%
Manager, Global Patient Safety Scientist
Regeneron Ireland · Dublin, Ireland · Manager
Function Therapeutic area Seniority Country
50%
Associate Director Global Patient Safety Sciences
Regeneron Ireland · Dublin, Ireland · Associate Director
Function Therapeutic area Adjacent seniority Country
45%
Senior Regulatory Affairs Manager
Gilead Sciences K.K. · Tokyo, Japan · Manager
Function Therapeutic area 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.