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New · posted Nov 1

Regeneron · Biotechnology

Temp Manager, Global Patient Safety Sciences

  • Tarrytown, NY
  • On-site
  • Full-time
  • Manager
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EmploymentFull-time
DeadlineOpen until filled

The role

SUMMARY: The Manager of Global Patient Safety (GPS) will play a key scientific role in safety strategies for molecules in clinical development and post-marketing phases. We will expect this to include safety data aggregation, review and analysis to support appropriate safety interpretation and benefit-risk assessment.

SCOPE:

N/A

What you need

Education

  • Master of science degree, PhD, or PharmD.

Experience

  • Previous safety or relevant clinical experience in the pharmaceutical industry required, typically with at least 5+ years of risk management or relevant clinical experience in pharmaceutical/ biotech industry or health authority
  • Clinical experience and/or Industry experience in the TA of interest is a plus

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

  • Complete signal detection activities in line with approved safety surveillance plan
  • Perform signal evaluation for any identified signals and author the safety evaluation reports
  • Manage preparation and review of safety documents including DSUR, PSUR, RMP, response to health authority or other queries
  • Prepare and deliver presentations at Signal Management Team (SMT) meetings; participate in clinical study team meetings for assigned molecules compounds
  • Participate in other risk management activities as appropriate for assigned compounds
  • We may ask you to represent GPS on cross-functional teams, including Regeneron Safety Oversight Committee (RSOC), Independent Data Monitoring Committees (IDMC) and other teams with members external to Regeneron
  • Experience in data manipulation and visualization (Excel, PIVOT tables, etc) for safety analysis
  • Actively participate in process improvement initiatives e.g. the development and maintenance of relevant SOPs, WIs and supporting documents

JOB REQUIREMENTS:

Pay and benefits

Regeneron didn't publish pay for this role

See what similar roles pay on Regulatory Jobs, or try the salary calculator.

  • 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, NYOn-siteOpen in Maps (opens in a new tab)

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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

Manager roles in the US26 roles publishing pay

Middle half $151,000 to $179,875, median $165,750
Annual base pay
Annual base payLowMedianHigh
All US$151,000$165,750$179,875

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. One step back

    Senior & Principal

    Often: Senior Safety Scientist · Clinical FSP Quality Manager

    $172K median17 open
  3. This role

    Manager

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

    $166K median30 open
  4. Next step

    Director

    Often: Director · Senior Medical Director

    $264K median92 open
  5. Later

    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 19 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

Documentation and SOPs: 3 linesRegulatory submissions: 2 linesQuality systems and risk: 4 linesData and digital systems: 1 lineClinical trial conduct: 2 linesCollaboration and leadership: 2 linesDocumentationSubmissionsQuality systemsData systemsClinical trialsTeamwork
  • Quality systems and risk4
  • Documentation and SOPs3
  • Regulatory submissions2
  • Clinical trial conduct2
  • Collaboration and leadership2
  • Data and digital systems1

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

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Temp Manager, Global Patient Safety Sciences at Regeneron

Open until filled.

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