When & where:
- Location: Tarrytown, NY, Cambridge, MA, or Warren, NJ
- Work Model: Primarily on-site with hybrid flexibility
Discover your role:
- Lead the scientific strategy behind clinical studies from design through execution and reporting
- Partner with Medical Directors and cross-functional teams to shape protocols, amendments, and study conduct
- Build deep expertise in disease biology, compound mechanism of action, and the competitive treatment landscape
- Author and review key trial documents, including expanded synopses, monitoring plans, and study reports
- Safeguard patient safety through ongoing clinical and medical data review
- Identify risks to study integrity early and drive practical mitigation strategies
- Represent Clinical Sciences on program teams, steering committees, and safety monitoring boards
- Champion consistent, high-quality data review practices across assigned studies
This role requires:
- MS, PhD, or PharmD in a related scientific field, plus 8+ years of pharmaceutical clinical drug development experience (other levels considered based on experience)
- Experience in Ophthalmology clinical trials preferred
- Proven knowledge of GCP, ICH guidelines, clinical trial design, and regulatory requirements
- Strong medical writing skills and clinical research methodology expertise
- Demonstrated success working cross-functionally in a matrix organization
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.
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)
$150,500.00 - $245,500.00
