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New · posted Nov 1

Regeneron · Biotechnology

Senior Manager, Clinical Scientist, Cardiovascular/Specialty Medicine

  • Tarrytown, NY +2 more
  • Hybrid
  • Full-time
  • Manager
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 Senior Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our global clinical development programs in cardiovascular, renal, and metabolic disease. In this role, you will help design, execute, and interpret clinical studies, safeguarding data integrity and patient safety while collaborating with Medical Directors and cross-functional study teams. 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

  • MS/PhD/PharmD in a related field with 8+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
  • Preferred: Experience in one or more of the following therapeutic areas: cardiovascular, renal, or metabolic disease
  • Preferred: Track record of clinical trial process improvements
  • Proven knowledge of the drug development process, GCP, ICH guidelines, study design, and clinical research methodology
  • Strong medical writing, analytical, and presentation skills, with the ability to communicate clear, concise messages
  • Demonstrated ability to influence within a team and cross-functionally in a matrix environment
  • Strong problem-solving and interpersonal skills, with the ability to resolve complex issues creatively and independently

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

  • Partner with Medical Directors to deliver the scientific expertise needed to design and run clinical studies
  • Contribute to clinical study teams, program team meetings, advisory boards, steering committees, and data/safety monitoring meetings
  • Support early and/or late-phase studies by helping develop protocol synopses and authoring or reviewing protocols and amendments
  • Author and review study documents, including medical monitoring plans, SAPs, informed consents, and clinical study report sections
  • Perform clinical and medical data review, including safety monitoring, to protect patient safety
  • Work with internal functions and external vendors to promote study integrity and consistent data review practices
  • Identify critical risks and recommend mitigations by analyzing how study objectives and design affect data analysis
  • Build and maintain deep knowledge of the disease area, mechanism of action, and drug landscape, while upholding FDA, EMA, ICH, and GCP standards

Pay and benefits

$150,500 – $245,500 a year

Employer provided
How this compares

$150,500.00 - $245,500.00

  • 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: Warren, NJ · Cambridge, MA

More jobs in Tarrytown, NY +2 more

Working conditions

When & where

  • Location: Tarrytown, NY, Warren, NJ, Cambridge, MA
  • Work model/flexibility: Primarily on-site with hybrid flexibility
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 level with the US median for Clinical Development roles at this level.

This roleEmployer provided

$150,500 to $245,500 a year

Manager roles in New York9 roles publishing pay

Middle half $198,500 to $198,500, median $198,500

Manager roles in the US13 roles publishing pay

Middle half $185,500 to $198,500, median $198,500
Annual base pay
Annual base payLowMedianHigh
This role$150,500—$245,500
New York$198,500$198,500$198,500
All US$185,500$198,500$198,500

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

Career trajectory

Where this role sits in Clinical Development

The general path across 263 open Clinical Development roles on Regulatory Jobs, with the titles they carry most. Not Regeneron's own promotion track.

  1. Earlier

    Associate & Specialist

    Often: 2027 Summer Intern Clinical Science, Medical Monitoring & Health Economics · Clinical Scientist- FSP

  2. One step back

    Senior & Principal

    Often: Clinical Scientist · Clinical Program Lead

    $187K median19 open
  3. This role

    Manager

    Often: Senior Manager, Clinical Scientist, Hematology · Senior Manager, Clinical Scientist, Immunology

    $199K median13 open
  4. Next step

    Director

    Often: Senior Director, Clinical Development · Director, Clinical Development

    $300K median211 open
  5. Later

    VP & Executive

    Often: Vice President, Clinical Development · Associate Vice President

    $395K median17 open

Skills DNA

What this role leans on

How many of the posting's 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.

GMP and compliance: 2 linesLab testing and methods: 2 linesDocumentation and SOPs: 5 linesQuality systems and risk: 1 lineData and digital systems: 1 lineClinical trial conduct: 7 linesCollaboration and leadership: 4 linesGMPLab testingDocumentationQuality systemsData systemsClinical trialsTeamwork
  • Clinical trial conduct7
  • Documentation and SOPs5
  • Collaboration and leadership4
  • GMP and compliance2
  • Lab testing and methods2
  • Quality systems and risk1
  • 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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Similar Clinical Development roles elsewhere

Senior Manager, Clinical Scientist, Cardiovascular/Specialty Medicine at Regeneron

Open until filled. $151K–$246K a year, employer provided.

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