Senior Manager, Clinical Sciences, Internal Medicine

Regeneron Pharmaceuticals • Tarrytown, NY

80d • $148,300 - $241,900 • Hybrid

About The Position

The Senior Manager, Internal Medicine, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and interpretation of study data of a clinical development program. The Sr. Manager leads in a matrix environment as part of a cross-functional team and may contribute to candidate development projects through early and/or late phase development. The Sr. Manager reports to the Associate Director, Clinical Sciences and collaborates closely with Medical Director(s) (MDs) to provide scientific expertise necessary to design and deliver on clinical studies and programs.

Requirements

• Bachelor's Degree; Advanced degree or equivalent education/degree in life science/healthcare preferred (PhD/MD/PharmD/MSc).
• ≥ 8 years of pharmaceutical clinical drug development experience.
• Proven knowledge of the drug development process, Good Clinical Practice, study design, clinical research methodology & medical writing skills.
• Knowledge of clinical development process, regulatory requirements and ICH/GCP guidelines.
• Proven track in clinical trial process improvements.
• Considerable organizational awareness, including significant experience working cross-functionally.

Nice To Haves

• Experience in one or more of the following therapeutic areas - cardiovascular, renal, metabolic disease - preferred.

Responsibilities

• Contributes to program team meetings, scientific advisory boards, study steering committees and data/safety monitoring meetings.
• Participates in collaborative activities with other departments.
• Member of the Clinical Study Team and Global Clinical SubTeam.
• Develops/maintains understanding of therapeutic disease area(s) and drug candidate including underlying disease biology, clinical manifestations and therapeutic standard practice.
• Applies basic scientific expertise to support initiation and execution of clinical research and development studies for early and/or late stage assets.
• Assists with development of the Expanded Synopsis and may author clinically relevant sections and review other scientific portions of clinical trial protocols and amendments.
• Assists with and may author/review documents related to trials, such as medical monitoring plans, SAPs, informed consents and clinical components of the Clinical Study Reports and may support the development of regulatory documents.
• Maintains compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical safety.
• Performs clinical/medical data review, including safety monitoring and activities and procedures that ensure patient safety.
• Collaborates with internal functions and external vendors to promote clinical study integrity.
• Exhibits strong analytical knowledge and skills to understand how study objectives and design impact data analysis.
• Supports identification and/or identifies critical risks and mitigations.
• Promotes consistent first line medical/clinical data review techniques and conventions across assigned studies.
• Reviews clinical data review plan and medical monitoring plan for assigned studies.

Benefits

• Health and wellness programs
• Fitness centers
• Equity awards
• Annual bonuses
• Paid time off for eligible employees at all levels

What This Job Offers

• Job Type: Full-time
• Career Level: Senior
• Industry: Chemical Manufacturing
• Education Level: Bachelor's degree