Vice President, Global Regulatory & Clinical Affairs will play a vital role in advancing LifeNet Health's mission by providing strategic leadership and expertise in regulatory and clinical affairs. The role will be responsible for developing new approaches for business objectives, driving operational effectiveness, and recommending solutions to reduce system complexities and inefficiencies.
Requirements
- Bachelor of Science: Engineering, Medical, Clinical or Biological Sciences
- Regulatory Affairs Certification: US, EU, and/or International
- TWELVE (12) Years – Personnel supervision with demonstrated leadership
- TEN (10) Years – Regulatory and Clinical Affairs experience in the medical devices or pharmaceutical industry with demonstrated increasing responsibility
- TEN (10) Years – Interfacing with FDA and other regulatory agencies in development and commercialization of new medical technologies
- FIVE (5) Years – Demonstrated success in US and International regulatory submission approvals, including IRBs, IDEs, PMAs, 510(k)
Benefits
- Affordable Medical, Dental, and Vision Coverage
- Profit Sharing Plan
- 403(b) Retirement Plan
- Paid Parental Leave
- Corporate Sponsored Events
- Generous Paid Time Off
- Flexible Work Program
- Tuition reimbursement
- Career & Leadership Development
- Wellness Program
- Employee Assistance Program (EAP)
- Incredible teammates