Senior Manager, Clinical Sciences – Internal Medicine

Regeneron Pharmaceuticals, Inc.; United States; Hybride; USD 180 000 - 240 000; Plein temps

Avantages offerts par ce poste

Health insurance

401(k) match

Bonus programs

Résumé du poste

Regeneron Pharmaceuticals, Inc. is seeking a Senior Manager, Clinical Sciences (Internal Medicine) to join its Clinical Sciences team.

Located primarily on-site with hybrid flexibility, the role supports global programs in cardiovascular, renal, and metabolic diseases, guiding design, execution, and interpretation of clinical studies to ensure data integrity and patient safety. The role collaborates with Medical Directors and cross-functional teams, developing protocols, monitoring plans, and

Qualifications

• MS/PhD/PharmD with 8+ years of pharmaceutical clinical drug development experience.
• Strong knowledge of GCP, ICH guidelines, study design, and clinical research methodology.
• Excellent medical writing, communication, and presentation skills.
• Ability to influence and lead cross-functional teams in a matrix environment.

Responsabilités

• Design, execute, and interpret clinical studies for cardiovascular, renal, and metabolic programs.
• Collaborate with Medical Directors and cross-functional study teams to safeguard data integrity and patient safety.
• Develop protocol synopses and author/review protocols and amendments for early and late-phase studies.
• Prepare and review study documents including medical monitoring plans, SAPs, and clinical study reports.

Connaissances

Medical writing

Analytical thinking

Presentation skills

Cross-functional influence

Formation

MS/PhD/PharmD in related field

Description du poste

Regeneron Pharmaceuticals, Inc. is seeking a Senior Manager, Clinical Sciences (Internal Medicine) to join its Clinical Sciences team.

Located primarily on-site with hybrid flexibility, the role supports global programs in cardiovascular, renal, and metabolic diseases, guiding design, execution, and interpretation of clinical studies to ensure data integrity and patient safety. The role collaborates with Medical Directors and cross-functional teams, developing protocols, monitoring plans, and