Regeneron Pharmaceuticals, Inc (USA) Posted July 15, 2026

Associate Director Global Patient Safety

Warren, United States Full time
Regulatory Affairs Associate Director

Regeneron Pharmaceuticals, Inc (USA) 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, PV Case Operations to join our Global Patient Safety team, supporting case processing across global development and commercial programmes in a hybrid work mode. In this role, you will lead vendor oversight, Individual Case Safety Report (ICSR) quality governance, and inspection readiness while collaborating with vendor teams, internal partners, license partners, auditors, and Health Authority inspectors. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

When & where:

This is an onsite position to be based in one of our US locations or in Uxbridge, UK (hybrid).

Discover your role:

Own accurate, timely case processing across global development and marketed products, per applicable regulations and Regeneron SOPs.

Lead vendor oversight for end-to-end ICSR receipt, processing, distribution, and submission.

Own ICSR quality standards covering narrative, case validity, and source document reconciliation.

Establish tiered quality review frameworks aligned to case complexity, risk, and product lifecycle stage.

Monitor submission timelines and vendor SLAs, maintain inspection readiness, and respond to audit findings.

Lead root cause analysis and own CAPAs through closure and effectiveness checks.

Evaluate AI-enabled tools for data ingestion, workflow automation, and metrics.

You mentor staff and communicate clearly with senior management and partners.

This role requires:

Pharmacy, nursing, or equivalent degree required; advanced degree preferred.

Typically 10 years of Pharmacovigilance, Drug Safety, or PV Quality experience in pharma or biotech.

Well-informed on FDA, EU, and ICH guidelines governing pharmacovigilance for clinical trial and post-marketing environments.

Experience managing teams on complex, cross-functional projects.

Proven ability to deliver organisational projects through individual contributors or other managers.

Strong communication and partner management skills, with ability to resolve and escalate complex issues.

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)

$157,200.00 - $256,600.00

Job details

Seniority
Associate Director
Function
Regulatory Affairs
Therapeutic area
Not listed
Location
Warren, United States
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 164 comparable Associate Director Regulatory Affairs roles across 48 biopharma companies.

164Comparable roles tracked
155Currently active
48Companies hiring similar roles
27Countries represented

Salary context

39 of 164 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 $157,200/yr – $256,600/yr
Peer group range $98,050 – $205,000 (median $180,500)

Where these roles are based

Top locations among the 164 comparable roles

United States60
India20
Ireland12
Poland11
Japan11
China7

+ 21 more countries

Seniority mix

164 of 164 peers have a known seniority level

Manager112
Senior27
Associate Director25

Therapeutic area mix

22 of 164 peers have a known therapeutic area; the rest are genuinely unlabeled, not hidden

Oncology7
Dermatology & Aesthetics6
Neuroscience5
Immunology4

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
AbbVie Mettawa, IL Associate Director
Same function Same seniority Same country
60%similar
AbbVie Mettawa, IL Associate Director
Same function Same seniority Same country
60%similar
AbbVie Mettawa, IL Associate Director
Same function Same seniority Same country
60%similar
AbbVie Associate Director
Same function Same seniority Same country

Open in 2 locations

Irvine, United StatesNorth Chicago, United States
60%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Associate Director
Same function Same seniority Same country
60%similar
E.R. Squibb & Sons,L.L.C. Princeton, United States Associate Director
Same function Same seniority Same country

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, Regulatory Affairs Advertising & Promotion - Digital & Corporate Communications
AbbVie · Mettawa, IL · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Regulatory Affairs US & Canada Strategy Lead – Facial Aesthetics - Device
AbbVie · Irvine, CA · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, Commercial Regulatory Affairs
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
Function Therapeutic area Seniority Country
60%
Associate Director, GRS Heme/Onc
E.R. Squibb & Sons,L.L.C. · Princeton, United States · Associate Director
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.