Medical Director - Cardio-Nephro Clinical Development

Regeneron Pharmaceuticals; Tarrytown (GA); Presencial; USD 285.000 - 386.000; Tempo integral

Resumo da vaga

Regeneron Pharmaceuticals in Tarrytown, NY, seeks a Medical Director to lead cardiovascular/metabolic clinical development. You will act as Medical Lead for trials, design study concepts, and oversee protocols, collaborating with cross-functional teams to ensure scientific excellence and patient safety.

The role requires an MD with board eligibility or certification and at least 2 years in pharma or equivalent research, with potential regulatory submission experience. On-site work is expected.

Qualificações

• MD with board eligibility or board certification in Cardiology, Nephrology, or Neurology preferred; relevant experience acceptable.
• At least 2 years pharmaceutical industry experience (academic research acceptable).
• Experience with regulatory submissions (CTD/dossier) in ICH regions is an advantage.

Responsabilidades

• Guide Global Clinical Study Team to deliver high-quality trials on time.
• Oversee medical monitoring of clinical trials to ensure patient safety and regulatory adherence.
• Lead clinical study and protocol development and present to internal and external stakeholders.
• Provide clinical and scientific leadership for data review, study reports, and publications.
• Collaborate with cross-functional partners to advance program goals and deliverables.
• Work with discovery teams to shape future targets and development opportunities.

Conhecimentos

MD degree

Board eligibility/certification

Clinical trial leadership

Formação

MD

Descrição da vaga

Regeneron Pharmaceuticals in Tarrytown, NY, seeks a Medical Director to lead cardiovascular/metabolic clinical development. You will act as Medical Lead for trials, design study concepts, and oversee protocols, collaborating with cross-functional teams to ensure scientific excellence and patient safety.

The role requires an MD with board eligibility or certification and at least 2 years in pharma or equivalent research, with potential regulatory submission experience. On-site work is expected.