Senior Manager, Clinical Scientist, Cardiovascular/Specialty Medicine

Regeneron Pharmaceuticals, Inc; Cambridge; On-site; GBP 112,000 - 183,000; Full time

Job summary

Regeneron Pharmaceuticals, Inc. is seeking a Senior Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting global programs in cardiovascular, renal, and metabolic disease.

You will design, execute, and interpret clinical studies, safeguard data integrity, and protect patient safety in collaboration with Medical Directors and cross-functional study teams. You will collaborate with Medical Directors to deliver scientific expertise, develop protocols, author

Qualifications

• MS/PhD/PharmD in related field with 8+ years of pharmaceutical clinical drug development experience
• Experience in one or more of the following therapeutic areas: cardiovascular, renal, or metabolic disease
• Proven knowledge of drug development processes, GCP, ICH guidelines, study design, and clinical research methodology

Responsibilities

• Design and run clinical studies in collaboration with Medical Directors
• Participate in cross-functional study teams, advisory boards, and data/safety monitoring meetings
• Develop protocol synopses and author/review protocols and amendments
• Author and review study documents including monitoring plans, SAPs, and clinical study report sections
• Perform clinical and medical data review, including safety monitoring
• Coordinate with internal functions and external vendors to maintain data integrity and study quality
• Identify risks and recommend mitigations by analyzing study objectives and design impact on data analysis
• Build deep knowledge of disease areas, mechanisms of action, and regulatory standards (FDA/EMA/ICH/GCP)

Skills

Clinical trial design

Medical writing

Data monitoring

Cross-functional collaboration

Education

MS/PhD/PharmD in related field

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 Senior Manager, Clinical Sciences (Internal Medicine) to join our Clinical Sciences team, supporting our global clinical development programs in cardiovascular, renal, and metabolic disease. In this role, you will help design, execute, and interpret clinical studies, safeguarding data integrity and patient safety while collaborating with Medical Directors 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:

• Partner with Medical Directors to deliver the scientific expertise needed to design and run clinical studies
• Contribute to clinical study teams, program team meetings, advisory boards, steering committees, and data/safety monitoring meetings
• Support early and/or late-phase studies by helping develop protocol synopses and authoring or reviewing protocols and amendments
• Author and review study documents, including medical monitoring plans, SAPs, informed consents, and clinical study report sections
• Perform clinical and medical data review, including safety monitoring, to protect patient safety
• Work with internal functions and external vendors to promote study integrity and consistent data review practices
• Identify critical risks and recommend mitigations by analyzing how study objectives and design affect data analysis
• Build and maintain deep knowledge of the disease area, mechanism of action, and drug landscape, while upholding FDA, EMA, ICH, and GCP standards

This role requires:

• MS/PhD/PharmD in a related field with 8+ years of pharmaceutical clinical drug development experience (other levels considered depending on experience)
• Preferred: Experience in one or more of the following therapeutic areas: cardiovascular, renal, or metabolic disease
• Preferred: Track record of clinical trial process improvements
• Proven knowledge of the drug development process, GCP, ICH guidelines, study design, and clinical research methodology
• Strong medical writing, analytical, and presentation skills, with the ability to communicate clear, concise messages
• Demonstrated ability to influence within a team and cross-functionally in a matrix environment
• Strong problem-solving and interpersonal skills, with the ability to resolve complex issues creatively and independently

Does this sound like you? 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