New · posted Nov 1
Regeneron · Biotechnology
Senior Manager, Clinical Scientist, Hematology
- Tarrytown, NY +2 more
- Hybrid
- Full-time
- Manager
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, Hematology Clinical Sciences to join our Clinical Sciences team, supporting our hematology clinical programs in a matrixed, cross-functional environment. In this role, you will contribute to the planning, execution, and data interpretation of clinical studies across early and late phase development, helping ensure the integrity of study data and the safety of patients. You will collaborate closely with Medical Directors and cross-functional partners as a member of the Clinical Study Team and Global Clinical SubTeam. 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
- Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc) and 8+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
- Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology, and medical writing
- Strong analytical, presentation, interpersonal, and problem-solving skills
- Significant experience working cross-functionally, with strong organizational awareness
- Preferred: Proven track record of clinical trial process improvements
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 provide the scientific expertise needed to design and deliver clinical studies and programs
- Contribute to program team meetings, advisory boards, steering committees, and data/safety monitoring meetings
- Build and maintain understanding of the disease area, drug candidate, mechanism of action, and drug landscape
- Assist with developing the Expanded Synopsis and author or review clinical sections of protocols, amendments, and study reports
- Author or review medical monitoring plans, SAPs, and informed consents, and support regulatory document development
- Perform clinical data review and safety monitoring, promoting consistent review practices across assigned studies
- Identify critical risks and recommend mitigations, while maintaining compliance with FDA, EMEA, ICH, and GCP guidelines
- Influence within and across teams with clear, concise communication and creative problem-solving
Pay and benefits
$150,500 – $245,500 a year
Employer provided$150,500.00 - $245,500.00
Annual bonuses
Equity awards
401(k) company match
Health and wellness programs
Medical, dental, vision 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 moreWorking conditions
When & where
- Location: Tarrytown, NY, Warren, NJ, or Cambridge, MA
- Work model: 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
Manager roles in New York9 roles publishing pay
Manager roles in the US13 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $150,500 | — | $245,500 |
| New York (middle half) | $198,500 | $198,500 | $198,500 |
| All US (middle half) | $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.
Skills DNA
What this role leans on
How many of the posting's 18 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct6
- Documentation and SOPs5
- Collaboration and leadership4
- GMP and compliance2
- Lab testing and methods2
- Quality systems and risk1
Regulatory intelligence
The rules behind this role
Frameworks and standards this posting's work falls under, matched from its own words, each linked to the official source.
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%
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