Nephrology Clinical Development Medical Director

Vertex Inc.

Boston (MA)

Híbrido

USD 204.000 - 306.000

Jornada completa

14 días+

Una candidatura completa en un minuto

Currículum y carta de presentación personalizados, listos para enviar.

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Ventajas ofrecidas por este puesto de trabajo

Total Rewards
Medical benefits
401(k)

Descripción de la vacante

Vertex seeks a Clinical Development Associate Medical Director to serve as the Medical Lead for clinical trials, overseeing strategy, design, execution and reporting. The role ensures scientific integrity and internal medical monitoring across studies, collaborating with Regulatory Affairs and Clinical Development Execution.

The candidate will provide clinical input to study documents, interact with external medical personnel, and participate in cross-functional teams.

Formación

  • MD/DO or equivalent medical degree required.
  • Approximately 8 years of basic or clinical research experience in academia or industry.
  • Experience interacting with regulatory authorities is a plus.
  • Proven ability to develop study protocols and regulatory documents.
  • Strong written and oral communication skills are essential.

Responsabilidades

  • Lead medical monitoring and scientific integrity across trials.
  • Participate in study protocol development, IND/CTA regulatory submissions, and reports.
  • Collaborate with cross-functional teams (Regulatory, Clinical Development, etc.).
  • Provide clinical input to study-related documents and analysis plans.
  • Represent Vertex to external medical personnel and in external reporting.

Conocimientos

Strong communication
Collaborative work
Global clinical research
Regulatory interaction
Biostatistics/pharmacology knowledge
Study design and protocols

Educación

MD or DO or equivalent ex-US medical degree
8+ years basic or clinical research experience

Descripción del empleo

Vertex seeks a Clinical Development Associate Medical Director to serve as the Medical Lead for clinical trials, overseeing strategy, design, execution and reporting. The role ensures scientific integrity and internal medical monitoring across studies, collaborating with Regulatory Affairs and Clinical Development Execution.

The candidate will provide clinical input to study documents, interact with external medical personnel, and participate in cross-functional teams.

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