Manager Clinical Affairs

📋 Description

• Lead clinical study programs: Plan, implement, manage, and report assigned clinical studies in
• Establish and manage program plans: Define detailed timelines, milestones, and objectives; monitor
• Oversee clinical quality and compliance: Develop, maintain, and optimize clinical quality systems
• Coordinate internal and external stakeholders: Direct and collaborate with cross-functional teams
• Develop clinical study documentation: Prepare and contribute to study protocols, statistical
• Support clinical affairs strategy: Contribute to the strategic direction, development, and

🎯 Requirements

• Relevant professional experience: At least five years of direct clinical and regulatory experience
• Clinical trial leadership: Demonstrated success in designing and conducting clinical trials
• Industry experience: Experience in the neurostimulation industry is preferred.
• Regulatory experience: Experience working with the U.S. Food and Drug Administration (FDA) and/or
• Education: Bachelor's degree or higher in a science, biomedical, health-related, or comparable
• Clinical data communication: Ability to synthesize complex clinical data and communicate findings

🎁 Benefits

• Full-time employment.
• Remote working arrangement, with the position listed in Minneapolis, Minnesota.
• Opportunity to contribute to clinical research and evidence generation for an innovative
• Collaborative, cross-functional working environment involving clinical, scientific, regulatory, and
• Opportunity to contribute to work focused on improving treatment options and patient outcomes.