New · posted Nov 1
Regeneron · Biotechnology
Senior Manager, Clinical Scientist, Genetics Medicine
- 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 to join our Clinical Sciences team within Regeneron Genetics Medicine, supporting early clinical development in a fast-paced, collaborative environment. In this role, you will contribute to clinical strategy and study execution from the discovery phase through Proof of Concept, helping translate genetic insights into potential new treatments. You will collaborate closely with your supervisor, Clinical Trial Managers, 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
- Bachelor’s degree and 8+ years of clinical research/development experience
- Preferred: PhD, PharmD, or Master’s degree in a biomedical subject
- Training as a scientist in the pharmaceutical or biotechnology sector, or in an academic or clinical setting
- Effective verbal and written communication and presentation skills
- Ability to work productively in a fast-paced, collaborative environment
- Demonstrated or potential critical thinking skills and sound decision-making
- Preferred: Experience in early-phase development, including First-In-Human and Proof of Concept studies
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.
Skills named in this posting
- Clinical research/development (8+ years)
- Clinical study protocols and amendments
- IND/IMPD submissions and investigator's brochures
- Medical monitoring and safety data review
- GCP and ICH compliance
- Early-phase development (First-In-Human, Proof of Concept)
- CRO and study team training
- Written and verbal communication
What you'll do
Discover your role
- Represent the clinical genetics medicine function on study teams, contributing medical and scientific expertise to compliant, high-quality trial execution
- Contribute to Clinical Study Concepts, protocols, and amendments, supported by literature research on indication selection, rationale, and endpoints
- Draft clinical sections of regulatory and clinical documents, including briefing books, IND/IMPD submissions, investigator’s brochures, consent forms, and study reports
- Review key study documents such as medical monitoring plans, statistical analysis plans, and data management materials
- Partner with Clinical Trial Managers to provide day-to-day clinical input and train study team and CRO personnel on clinical aspects of the trial
- Support medical monitoring, investigator queries, safety narratives, and trend analysis of safety and efficacy data
- Organize steering committees, advisory boards, data safety monitoring boards, and consultations with global subject matter experts
- Identify program, trial, and data risks and implement mitigation strategies, while ensuring compliance with FDA, EMEA, ICH, and GCP guidelines
Pay and benefits
$150,500 – $245,500 a year
Employer provided$150,500.00 - $245,500.00
Annual bonuses and 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 moreWorking 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
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 20 duty, requirement and summary lines touch each area. The posting's emphasis, not a proficiency score.
- Clinical trial conduct6
- Collaboration and leadership6
- Documentation and SOPs2
- Investigations and CAPA2
- GMP and compliance1
- Regulatory submissions1
- Data and digital systems1
- Clinical research/development (8+ years)
- Clinical study protocols and amendments
- IND/IMPD submissions and investigator's brochures
- Medical monitoring and safety data review
- GCP and ICH compliance
- Early-phase development (First-In-Human, Proof of Concept)
- CRO and study team training
- Written and verbal communication
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.
- ICHICH quality guidelines(official source, opens in a new tab)Q1 stability, Q2(R2) analytical validation, Q7, Q9 risk management, Q10 quality systems
- ICHICH E6 good clinical practice(official source, opens in a new tab)The international standard for the conduct of clinical trials
- FDAFDA IND(official source, opens in a new tab)Investigational New Drug applications
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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