New · posted Nov 1
Regeneron · Biotechnology
Senior Manager, Clinical Study Lead, Inflammation & Immunology
- Tarrytown, NY
- 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 Clinical Study Lead to join our Clinical Trial Management team, accountable for the global execution of large and complex clinical trials from study design through close out. In this role, you will lead cross-functional study teams and oversee CROs and vendors, ensuring studies are delivered on time, on budget, and in accordance with ICH/GCP and Regeneron SOPs. You will also supervise Clinical Trial Management staff and drive process improvement initiatives. 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 relevant clinical trial experience
- Extensive experience in global clinical trial operations, with knowledge of ICH/GCP and regulatory guidelines
- Line management experience and the ability to build, lead, and develop productive study teams
- Strong budget management, vendor management, and negotiation skills
- Exceptional interpersonal, communication, and influencing skills across a wide range of stakeholders
- Preferred: Advanced proficiency in trial management systems (CTMS, EDC, IVRS/IWRS) and MS applications
- Preferred: Awareness of relevant industry trends and experience driving process improvement
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
What you'll do
Discover your role
- Lead the cross-functional study team as the primary point of contact for assigned studies, with high independence and accountability for timelines, budget, and quality
- Provide operational input into protocol development and key study documents, including data management, monitoring, and statistical analysis plans
- Lead feasibility assessments, site evaluation and selection, investigator meetings, and patient recruitment and retention strategies
- Select, contract, and oversee CROs and third-party vendors to ensure delivery against the scope of work
- Manage study budgets and timelines, identify risks, and escalate issues with clear mitigation plans
- Oversee data quality, protocol deviations, and study systems such as CTMS and TMF to keep studies audit and inspection ready
- Manage study close-out activities and contribute to clinical study reports and lessons learned
- Supervise, coach, and develop Clinical Trial Management staff while driving innovation and process improvement across the department
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, life and disability insurance
Paid time off
Where you'll work
Tarrytown, NYHybridOpen in Maps (opens in a new tab)
More jobs in Tarrytown, NYWorking conditions
When & where
- Location: Tarrytown, NY, Warren, NJ, Cambridge, MA
- Work model/flexibility: Primarily on-site with hybrid flexibility
- Travel percentage: Up to 25%
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 3, 2026
Salary intelligence
How the pay compares
This role's midpoint is 21% above the US median for Clinical Trial Management roles at this level.
This roleEmployer provided
Manager roles in New York6 roles publishing pay
Manager roles in the US45 roles publishing pay
| Annual base pay | Low | Median | High |
|---|---|---|---|
| This role | $150,500 | — | $245,500 |
| New York (middle half) | $150,750 | $169,500 | $191,250 |
| All US (middle half) | $149,000 | $163,000 | $175,000 |
This role: Regeneron's own published range. Comparisons: the base pay employers published on open Clinical Trial Management roles at the same level on Regulatory Jobs, November 3, 2026. Nothing is estimated.
Career trajectory
Where this role sits in Clinical Trial Management
The general path across 70 open Clinical Trial Management 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 conduct10
- Collaboration and leadership6
- GMP and compliance3
- Documentation and SOPs3
- Quality systems and risk3
- Investigations and CAPA2
- Data and digital systems1
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%
- Quality66 40%
- Regulatory28 17%
By level
- Associate & Specialist53 33%
- Director50 31%
- Manager46 28%
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Senior Manager, Clinical Study Lead, Inflammation & Immunology at Regeneron
Open until filled. $151K–$246K a year, employer provided.