Senior Manager, Clinical Scientist, Genetics Medicine

Regeneron Pharmaceuticals; Cambridge; Presencial; GBP 113.000 - 184.000; Jornada completa

Descripción de la vacante

Regeneron Pharmaceuticals seeks a Senior Manager to join our Clinical Sciences team within Regeneron Genetics Medicine, supporting early development in a fast-paced, collaborative environment. You will contribute to clinical strategy and study execution from discovery through Proof of Concept, translating genetic insights into potential new treatments.

Collaborate with your supervisor, Clinical Trial Managers, and cross-functional study teams to ensure compliant, high-quality trial execution and

Formación

• 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.

Responsabilidades

• 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

Conocimientos

Clinical research

Regulatory familiarity

Communication skills

Team collaboration

Critical thinking

Early-phase experience

Educación

Bachelor’s degree

PhD/PharmD/Master’s in biomedical subject

Descripción del empleo

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.

When & where:

• Location: Tarrytown, NY, Warren, NJ, Cambridge, MA
• Work model/flexibility: Primarily On-site with hybrid flexibility

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

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

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)

$150,500.00 - $245,500.00