Senior Neurovascular Clinical Research Lead

Regulatory Jobs; Fridley (MN); Híbrido; USD 106.000 - 158.000; Jornada completa

Ventajas ofrecidas por este puesto de trabajo

Flexible onsite work model

Descripción de la vacante

Medtronic is seeking a Senior Clinical Research Specialist to lead development of clinical, scientific, and regulatory documentation, supporting regulatory submissions and evidence generation for neurovascular therapies.

The role requires a Bachelor's degree in a technical field with 4+ years of clinical research or regulatory writing, and involves collaboration across Clinical, Regulatory, Quality, Marketing, and cross-functional teams in a hybrid onsite model with up to ~25% travel.

Formación

• Bachelor’s degree in a technical discipline with 4+ years of relevant clinical research or regulatory writing experience.
• Experience authoring clinical, scientific, or regulatory documentation for regulated healthcare products.
• Experience collaborating with cross-functional teams in a regulated medical device environment.
• Ability to analyze and communicate clinical data to diverse stakeholders.

Responsabilidades

• Author and lead clinical, scientific, and regulatory documents such as protocols, study reports, and regulatory submissions.
• Develop evidence strategies aligned with program objectives and regulatory requirements.
• Collaborate with Clinical, Research & Development, Regulatory, Quality, Marketing, and Health Economics teams.
• Summarize and present clinical data through reports, presentations, and evidence summaries.

Conocimientos

Clinical research

Regulatory writing

Medical device experience

Scientific writing

Cross-functional collaboration

Educación

Bachelor's degree in technical discipline

Advanced degree

Descripción del empleo

Medtronic is seeking a Senior Clinical Research Specialist to lead development of clinical, scientific, and regulatory documentation, supporting regulatory submissions and evidence generation for neurovascular therapies.

The role requires a Bachelor's degree in a technical field with 4+ years of clinical research or regulatory writing, and involves collaboration across Clinical, Regulatory, Quality, Marketing, and cross-functional teams in a hybrid onsite model with up to ~25% travel.