Summary written by USA Jobs 24 from Regeneron's advert and our data on 17,030 current US jobs. How we check every job
At a glance
Regeneron is hiring a Senior Director, Global Patient Safety - Rare Disease in Cambridge, MA; Tarrytown, NY. It is a full-time role in Healthcare & Life Sciences, asking for at least 5 years of experience, first listed on November 1. The advertised pay is $242,000–$403,300 a year. Regeneron has 99 other openings in the US, 2 of them in Cambridge, MA. Across all employers on USA Jobs 24 there are 17 Healthcare & Pharma openings in Cambridge, MA today; the typical one asks for 5 years and advertises about $273,000 a year at the midpoint.
How the pay compares
Regeneron advertises $242,000 to $403,300 a year, a midpoint of $322,650 a year. Where an offer lands in a range usually depends on experience and on the exact location. That is higher than about 89% of the 56 healthcare & pharma jobs in Massachusetts that publish a yearly rate on USA Jobs 24, where the typical midpoint is $215,000 a year. To see roughly what this leaves after federal and Massachusetts tax, try our take-home pay calculator.
Before you apply
- Check it is still open. We found this job on Regeneron's Workday site on November 1 and checked it again November 4, 5:17 AM ET. When an employer takes a job down, we remove it at our next daily update.
- Check the location works for you. This role is based in Cambridge, MA (or one of 1 other locations). If you would need to move, ask whether relocation help is offered.
- Match the experience. The advert asks for at least 5 years of experience. If you are a little short, a close match on the skills in the advert can still win an interview.
- Know your number. Decide the lowest offer you would accept before the first call. Our salary negotiation guide explains how to ask for more.
- Apply only through Regeneron's own site. Our Apply button goes straight to Regeneron's Workday page. If anyone contacts you about this job and asks for money, gift cards or bank details, stop and check it with our scam checker. Read how to spot a fake job offer.
About hiring at Regeneron
Regeneron has 100 openings on USA Jobs 24 today across 8 states. Most are in healthcare & pharma (23), software & IT (13) and data & AI (13). The biggest locations are Tarrytown, NY (40), Armonk, NY (11) and Cambridge, MA (3). 8% of them are remote, 30% are open to entry-level candidates and 98% show pay. We collect Regeneron's jobs every day straight from its own careers system (Workday), never from job boards or agencies.
The employer's advert
This is Regeneron's own description of the job, copied word for word from its careers site. We have not edited it.
Show the full advert from RegeneronHide the advert992 words
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 Senior Director to join our Global Patient Safety team.
This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
- Work Location: Tarrytown, NY, Warren, NJ or Cambridge, MA
- 4 days per week on site
- 25% Travel may be required
Discover your role:
- Reporting to the Global Patient Safety (GPS) Therapeutic Area (TA) Head, the Senior Director GPS Lead, serves as the first point of contact (POC) for all safety related issues for the compound(s) assigned within the therapeutic area (TA).
- This position is directly responsible for all aspects of GPS activities for assigned compounds and products in support of safety surveillance, signal management, communication of the safety profile as appropriate for the stage in the asset lifecycle, benefit risk assessment, safety responses to regulatory agency queries, safety documents (DSURs, PSURs, development RMPs, RMPs, etc.) and the review of clinical documents (Investigator Brochures, protocols, clinical study reports, etc.)
- The GPS Lead is the GPS representative on the cross functional Strategic Program Team (SPT) and the Chair of the Safety Management Team (SMT) for the compound.
- The GPS Lead leads the safety strategy and ensures the optimal support from within GPS and works collaboratively with stakeholders to deliver the safety profile and the safety strategy.
- Assigned compounds will include a variety obesity/metabolism products in various stages of development.
- This position requires the ability to work with and influence colleagues in a matrix environment within and external to GPS including senior management.
- Leads cross-functional Safety Monitoring Team (SMT) activities Represent GPS for assigned compounds on cross-functional teams, including Regeneron’s Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC), Strategic Program Team (SPT) and other teams with members external to Regeneron (alliance partners, CROs)
- Serves as delegate as needed for GPS Therapeutic Area Head, General Medicine
- Proactively identify and develop safety strategies and planning for non-compound specific GPS activities (mechanism of action etc.)
- Act as a resource for medical review for complex ICSRs, and other data sources of assigned compounds
- Actively participate in the development and maintenance of relevant SOPs, working practices and guides
- Actively participates in continuous improvement activities within both the TA and the GPS organization, including cultivating cross functional relationships and mentoring junior safety scientists
This role requires:
- 5+ years of total relevant experience in PV and/or relevant medical field with PharmD / PhD / MD degree
- 15+ years of total relevant experience in PV and/or relevant medical field or equivalent in lieu industry experience in drug safety including significant experience with PSURs/ DSURs/(d) RMPS; or in clinical development with demonstrated achievements in safety (ex. supporting an ISS; responsible for CSR content)
- Demonstrated experience in specialty TAs incorporating advanced therapies, such as gene therapy into pharmacovigilance practices
- Ability to apply and provide critical analysis of relevant FDA, EU and ICH guidelines, initiatives and regulations governing pharmacovigilance activities for both clinical trial and post-marketing environments required.
- Function as a subject matter expert internal and external to GPS for assigned compounds with relevant clinical industry experience in the therapeutic area of interest.
- Thorough understanding of drug development and context as applicable to safety surveillance activities
- A proven ability to lead and develop a diverse team of safety professionals in a constructive, goal-oriented environment.
- An ability to work across organizational levels, effectively communicating safety viewpoints and findings as required, and recommended risk management and minimization activities.
- Ability to utilize GPS safety database for purposes of medical case review and simple queries.
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)
$242,000.00 - $403,300.00USA Jobs 24 copied this listing from Regeneron's official careers site on November 1, 2026 and checked it again November 4, 5:17 AM ET. Regeneron will never ask you to pay to apply or to buy equipment with a check they send you. If anyone does, it is a scam.
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