Associate Director, Clinical Scientist, Genetics Medicine

Regeneron Pharmaceuticals; Cambridge; Híbrido; GBP 129.000 - 216.000; Jornada completa

Descripción de la vacante

Regeneron Pharmaceuticals is seeking an Associate Director, Clinical Sciences to lead design, execution, and interpretation of clinical studies across early and late phase programs. You will collaborate with Medical Directors, regulatory teams and cross-functional partners to advance promising candidates while ensuring patient safety and data integrity.

The role requires a PhD/MD-like background or advanced life sciences degree, 10+ years in pharmaceutical development, and demonstrated

Formación

• Bachelor’s degree and 10+ years of pharmaceutical clinical drug development experience
• Proficient knowledge of the drug development process, ICH/GCP guidelines, study design, and clinical research methodology
• Demonstrated leadership in conducting global clinical trials and executing clinical programs
• Strong cross-functional leadership, interpersonal, and problem-solving skills in a matrix environment

Responsabilidades

• Lead or support clinical science strategy for a program, serving as lead Clinical Scientist or delegate to the Therapeutic Area Lead
• Partner with Medical Directors to design and deliver clinical studies grounded in disease biology and current literature
• Develop the Expanded Synopsis and author or review the clinical sections of protocols, amendments, and study reports
• Prepare medical monitoring plans, SAPs, and informed consents, and resolve cross-functional comments with minimal guidance
• Perform clinical data review and safety monitoring to protect patient safety and data integrity
• Present at program team meetings, advisory boards, steering committees, DMCs, and investigator meetings
• Identify risks, design mitigation strategies, and drive process improvements across studies
• Influence across functions and mentor junior colleagues with confidence, creativity, and professional diplomacy

Conocimientos

Leadership

Cross-functional collaboration

Medical writing

Problem-solving

Interpersonal skills

Educación

Bachelor's degree in Life Sciences

Advanced degree (PhD/MD/PharmD/MSc) preferred

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 an Associate Director, Clinical Sciences to join our Clinical Development Unit, supporting our clinical programs in a matrixed, cross-functional environment. In this role, you will lead the design, execution, and scientific interpretation of clinical studies across early and late phase development, ensuring the integrity of study data and the safety of patients. You will collaborate closely with Medical Directors, regulatory, and other cross-functional partners to move promising candidates forward. 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:

• Lead or support clinical science strategy for a program, serving as lead Clinical Scientist or delegate to the Therapeutic Area Lead
• Partner with Medical Directors to design and deliver clinical studies grounded in disease biology and current literature
• Develop the Expanded Synopsis and author or review the clinical sections of protocols, amendments, and study reports
• Prepare medical monitoring plans, SAPs, and informed consents, and resolve cross-functional comments with minimal guidance
• Perform clinical data review and safety monitoring to protect patient safety and data integrity
• Present at program team meetings, advisory boards, steering committees, DMCs, and investigator meetings
• Identify risks, design mitigation strategies, and drive process improvements across studies
• Influence across functions and mentor junior colleagues with confidence, creativity, and professional diplomacy

This role requires:

• Bachelor’s degree and 10+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
• Proficient knowledge of the drug development process, ICH/GCP guidelines, study design, and clinical research methodology
• Demonstrated leadership in conducting global clinical trials and executing clinical programs
• Strong cross-functional leadership, interpersonal, and problem-solving skills in a matrix environment
• Solid medical writing skills
• Preferred: Advanced degree in life science or healthcare (PhD, MD, PharmD, or MSc)
• Preferred: Proven track record of clinical trial process improvements and experience across early and late phase development

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.

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)

$176,100.00 - $287,300.00