Executive Director, Global Patient Safety Sciences Delivery

Regeneron Pharmaceuticals, Inc; Dublin; On-site; EUR 172,500 - 288,300; Full time

Benefits offered by this job

Annual bonuses

Health and wellness programs

Paid time off

Job summary

Regeneron Pharmaceuticals, Inc is seeking an Executive Director to join their Patient Safety team in Dublin, Ireland. The role involves overseeing Safety Sciences operations and ensuring compliance and quality management across therapeutic areas.

The ideal candidate will have at least 17 years of experience in pharmacovigilance or a relevant clinical role, with strong leadership and communication skills. This position offers a competitive salary and the opportunity to make a meaningful difference in patient care.

Qualifications

• 17+ years of total experience in PV or relevant clinical experience in the pharmaceutical industry.
• 6+ years of leading a team and people management experience.
• Preferred experience with operations oversight in a global patient safety organization.

Responsibilities

• Define strategy for execution of core activities across all products.
• Oversee training programs for GPS Safety Sciences.
• Ensure compliance and quality management of Safety Sciences Operations.

Skills

Leadership capabilities

Strong communication skills

Organizational skills

Attention to detail

Education

M.D., PA, PhD or PharmD Degree

Board Certification or equivalent

MBA (preferred)

Job description

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 Executive Director to join our Patient Safety team.

The Executive Director, Global Patient Safety Sciences Delivery serves as the key point of contact for all Safety Sciences operations and risk‑related responsibilities across all Therapeutic Areas (TAs). This role is responsible for driving consistency across the portfolio for standard activities performed by the Safety Scientists (e.g., data transformation, safety surveillance, SMT preparation, early draft of aggregate reports, signal evaluations, label enhancement justifications). This role is also responsible for the processes and written procedures that underpin the safety governance, and other fundamental processes within Safety Sciences. The Executive Director, Global Patient Safety Sciences Delivery requires the ability to work cross‑functionally, partnering with the Safety Sciences TAHs and other leaders, and will serve as a member of the GPS Leadership Team (GPS LT). The Executive Director is also responsible for the development and management of their 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: Dublin, Ireland
• Travel: As needed

Discover your role:

• Define the strategy to ensure standardization and consistency in execution of core activities (e.g., signal detection, authoring sections for safety documents) across all products and TAs through development of common practices, processes and templates.
• Oversee relevant training programs for GPS Safety Sciences, including a standardized training curriculum, proficiency matrix and knowledge management repository.
• Enable the Global Capability Center (GCC) to operate more efficiently and scale with the demands of the business.
• Develop innovative approaches to delivering core activities that integrate new technologies, including AI.

Operational Delivery Oversight:

• Ensure compliance and quality management of Safety Sciences Operations activities, including compliance with all regulations and establishment of SOPs and associated monitoring tools.
• Oversee all aspects of signal detection coordination and signal management process across all TAs, including Safety Monitoring Team (SMT), Safety Surveillance Plan (SSP) and Signal Evaluation Report (SER).
• Coordinate and support high‑quality, timely and compliant delivery of benefit‑risk assessment for periodic safety reports (e.g., DSURs, PSURs) and support Safety Sciences Strategy in contributing Medical and Safety perspective to the GPS portfolio of documents (e.g., ARM, RMP, SMP) where required.
• Set and oversee the framework for aggregate safety data analysis to ensure effective coordination and delivery.

Cross‑Functional Partnership:

• Serve as strategic point of contact to enable SS operational delivery in partnership with TAHs and GPS Leads.
• Partner with key Regeneron interfaces (e.g., Clinical, Regulatory, Med Affairs, Biostats & Data Management).

Talent Development & Organizational Leadership:

• Build, coach and scale a high‑performing team, and drive succession planning and talent pipelines.
• Lead talent strategy and leadership development initiatives that strengthen capabilities across the organization.

This role requires:

• Minimum M.D., PA, PhD or PharmD Degree; Board Certification or equivalent in relevant clinical specialty, MBA is an advantage.
• 17+ years total experience in PV or relevant clinical experience in the pharmaceutical industry required.
• 6+ years of leading a team and people management experience.
• Preferred experience with oversight of operations within a global patient safety organization.
• Strong attention to detail with the ability to assess and optimize Safety operations processes, drive consistency and ensure high‑quality, compliant execution across activities.
• Strong leadership capabilities and presence, interpersonal, verbal and written communication skills, organizational and workload planning skills along with the ability to manage multiple different projects simultaneously.

Salary Range (annually)

€172,500.00 - €288,300.00

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.

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.