Manager, Clinical Scientist, Internal Medicine

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

Location: Tarrytown, NY

Work model: Primarily on-site with hybrid flexibility

Discover your role

• Support the planning, execution, and evaluation of early- and late-phase clinical studies
• Partner with Medical Directors to deliver scientific expertise for study and program design
• Contribute to program team meetings, advisory boards, steering committees, and safety monitoring meetings
• Develop a deep understanding of the disease area, drug mechanism, and competitive landscape
• Author and review key study documents, including protocol sections, monitoring plans, SAPs, informed consents, and Clinical Study Report components
• Review clinical and safety data to protect patient safety and ensure data integrity
• Identify study risks and propose practical mitigations
• Work with internal teams and external vendors to uphold study quality and compliance with FDA, EMA, ICH, and GCP standards

Requirements

• MS, PhD, or PharmD in a related field
• 5+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)
• Working knowledge of the drug development process, GCP, study design, and clinical research methodology
• Strong analytical, communication, and presentation skills, with the ability to influence within and across teams
• Demonstrated ability to solve complex problems independently and work effectively in a matrix environment

Preferred

• experience in cardiovascular, renal, or metabolic disease
• medical writing skills and a track record of clinical trial process improvements

Salary Range (annually) $128,600.00 - $210,000.00

Benefits

• 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
• family support 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.

Regeneron is a leading biotechnology company that invents life-transforming medicines for people with serious diseases. Founded and led for over 30 years by physician-scientists, our unique ability to repeatedly and consistently translate science into medicine has led to nine FDA-approved treatments and numerous product candidates in development, almost all of which were homegrown in our laboratories. Our medicines and pipeline are designed to help patients with eye diseases, allergic and inflammatory diseases, cancer, cardiovascular and metabolic diseases, neurology, infectious diseases and rare diseases.

Regeneron is also proud of award winning culture of innovation, being recognized as a Great Place to Work in 2021, Fast Company’s Best Workplace for Innovators in 2020, and Forbes JUST companies in 2020, among others.

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 … [benefit list repeated above] …

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.