
Manager, Clinical Scientist, Internal Medicine
Tarrytown, NY · HybridJob$129–210K/yrSeen todaySeen in employer's feed today
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Job overview
Regeneron seeks a Manager, Clinical Sciences (Internal Medicine) to support cardiovascular, renal, and metabolic disease programs. The role contributes to the design, execution, and interpretation of clinical studies across development phases, working with Medical Directors and cross-functional teams. It is primarily on-site with hybrid flexibility and requires an advanced degree and at least five years of pharmaceutical clinical drug development experience; disease-area experience and medical writing are preferred.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
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 Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our cardiovascular, renal, and metabolic disease programs. In this role, you will help design, execute, and interpret clinical studies that advance our development pipeline while collaborating with Medical Directors and cross-functional teams. This position offers the opportunity to contribute to a fast-growing, science-driven organization making a meaningful difference to patients worldwide.
When & where:
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Location: Tarrytown, NY
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Work model: Primarily on-site with hybrid flexibility
Discover your role:
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Support the planning, execution, and evaluation of early- and late-phase clinical studies
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Partner with Medical Directors to deliver scientific expertise for study and program design
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Contribute to program team meetings, advisory boards, steering committees, and safety monitoring meetings
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Develop a deep understanding of the disease area, drug mechanism, and competitive landscape
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Author and review key study documents, including protocol sections, monitoring plans, SAPs, informed consents, and Clinical Study Report components
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Review clinical and safety data to protect patient safety and ensure data integrity
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Identify study risks and propose practical mitigations
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Work with internal teams and external vendors to uphold study quality and compliance with FDA, EMA, ICH, and GCP standards
This role requires:
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MS, PhD, or PharmD in a related field
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5+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)
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Working knowledge of the drug development process, GCP, study design, and clinical research methodology
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Strong analytical, communication, and presentation skills, with the ability to influence within and across teams
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Demonstrated ability to solve complex problems independently and work effectively in a matrix environment
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Preferred: experience in cardiovascular, renal, or metabolic disease
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Preferred: medical writing skills and a track record of clinical trial process improvements
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.
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.
Salary Range (annually)
$128,600.00 - $210,000.00
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