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New · posted Nov 1

Regeneron · Biotechnology

Director, Pharmacovigilance Hub - Americas

  • Tarrytown, NY +2 more
  • Hybrid
  • Full-time
  • Director
Save
EmploymentFull-time
DeadlineOpen until filled

The role

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 Director, Pharmacovigilance Hub to join our Global Patient Safety Operations team. The Director, PV Hub oversees country and/or regional level PV execution within their assigned region and ensures that local safety activities are performed in accordance with global standards, local regulatory requirements are met, and all country-generated safety data are accurately and timely integrated into the global PV system. This role serves as the escalation point for local execution issues and as the conduit between local operations and global oversight functions.

This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.

What you need

This role requires

  • Minimum Bachelor’s Degree (Advanced Degree preferred) with 12+ years of PV experience and demonstrated achievements in patient safety
  • Experience supporting regulatory inspections, audits, and quality issue management at the country or regional level
  • Preferred experience with AI technologies
  • Ability to coordinate across functions and cultures, operating effectively as an execution and escalation lead rather than a policy owner
  • Strong organizational and communication skills, with the ability to surface local risks early and drive resolution through global governance channels
  • Experience working within LATAM, US and Canadian markets strong preferred

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.

What you'll do

Discover your role

  • Maintain a comprehensive understanding of local legislation and Health Authority requirements and keep Worldwide Operations Office (WWOO) leadership informed of updates or changes to local requirements or processes (e.g., SOP addenda, safety communications, labeling updates, and local submission requirements) in alignment with country-specific regulatory requirements
  • Track local process status, changes, and risks to drive consistency and continuous improvement for hub’s geographic markets, including maintaining and monitoring via common tool (e.g., tracker, dashboard)
  • Develop innovative approaches to delivering on core activities that integrate in new technologies, including AI
  • Ensure country compliance with the global PV quality system, supporting inspections, audits, CAPAs, and timely resolution of deviations or non-compliance
  • Serve as local safety PoC to coordinate with global GPS (e.g., PV Enablement, CER, SS) and non-GPS (e.g., Med Affairs, Regulatory) teams to:
  • Guide and inform global teams on local requirements and ensure compliance with local legislations
  • Coordinate with other PV hub(s) as needed for contributions to activities and/or local documentation
  • Shape compliant programs that provide high quality adverse event reports
  • Build, coach, and scale a high-performing team, and drive succession planning and talent pipelines

Pay and benefits

$183,100 – $305,200 a year

Employer provided
How this compares

$183,100.00 - $305,200.00

  • Annual bonuses or incentive plans

  • Equity awards

  • 401(k) company match

  • Health and wellness programs

  • Medical, dental, vision, life and disability insurance

  • Paid time off

Where you'll work

Tarrytown, NY +2 moreHybridOpen in Maps (opens in a new tab)

Also posted for: Cambridge, MA · Warren, NJ

More jobs in Tarrytown, NY +2 more

Working conditions

When & where

  • Work Location: Tarrytown, NY, Cambridge MA or Warren, NJ
  • 4 days per week on site
Equal opportunity, accessibility and legal noticesRegeneron's statements, word for word

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.

Job intelligence

The context around this role

Live data · November 1, 2026

Salary intelligence

How the pay compares

This role's midpoint is 8% below the US median for Clinical Safety & Pharmacovigilance roles at this level.

This roleEmployer provided

$183,100 to $305,200 a year

Director roles in New York9 roles publishing pay

Middle half $273,500 to $273,500, median $273,500

Director roles in the US90 roles publishing pay

Middle half $218,875 to $281,000, median $264,000
Annual base pay
Annual base payLowMedianHigh
This role$183,100—$305,200
New York$273,500$273,500$273,500
All US$218,875$264,000$281,000

This role: Regeneron's own published range. Comparisons: the base pay employers published on open Clinical Safety & Pharmacovigilance roles at the same level on Regulatory Jobs, November 1, 2026. Nothing is estimated.

Career trajectory

Where this role sits in Clinical Safety & Pharmacovigilance

The general path across 162 open Clinical Safety & Pharmacovigilance roles on Regulatory Jobs, with the titles they carry most. Not Regeneron's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: Associate, Pharmacovigilance Operations/Drug Safety · Clinical Safety Coordinator

    $92K median10 open
  2. Earlier

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $172K median17 open
  3. One step back

    Manager

    Often: Senior Manager, Clinical Quality Assurance · Clinical FSP Quality Manager

    $166K median30 open
  4. This role

    Director

    Often: Director · Senior Medical Director

    $264K median92 open
  5. Next step

    VP & Executive

    Often: Head of Multiple Myeloma & AML, Oncology · Head of Patient-Facing Quality Assurance

    $347K median13 open

Skills DNA

What this role leans on

How many of the posting's 21 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 3 linesDocumentation and SOPs: 3 linesInvestigations and CAPA: 1 lineRegulatory submissions: 1 lineQuality systems and risk: 2 linesClinical trial conduct: 1 lineCollaboration and leadership: 7 linesGMPDocumentationInvestigationsSubmissionsQuality systemsClinical trialsTeamwork
  • Collaboration and leadership7
  • GMP and compliance3
  • Documentation and SOPs3
  • Quality systems and risk2
  • Investigations and CAPA1
  • Regulatory submissions1
  • Clinical trial conduct1

Company hiring pulse

Regeneron on Regulatory Jobs

163
Open roles
140
Distinct roles
11
Locations

By discipline

  • Clinical69 42%
  • Quality67 41%
  • Regulatory27 17%

By level

  • Associate & Specialist53 33%
  • Director49 30%
  • Manager46 28%
See all 163 Regeneron roles

More roles at Regeneron

All 163 Regeneron roles

Similar Clinical Safety & Pharmacovigilance roles elsewhere

Director, Pharmacovigilance Hub - Americas at Regeneron

Open until filled. $183K–$305K a year, employer provided.

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