Medtronic is looking to solve healthcare access and equity issues by innovating and developing new medical technologies. This role supports clinical studies to bring these innovations to market.
Requirements
- Prior experience in clinical trials with medical devices
- Demonstrated ability to problem solve
Responsibilities
- Provides study execution support for sponsored clinical studies primarily at the site level.
- Oversees and resolves operational aspects of clinical trials in conjunction with project teams and in accordance with standard operating procedures (SOP), good clinical practice (GCP), and specific country regulations, and may prepare clinical trial budgets.
- May be responsible for clinical supply operations, site, and vendor selection.
- Represents Medtronic from a clinical research perspective within the country/region and also collects feedback from local customers and authorities.
- Drives local evidence dissemination & awareness.
- Oversees, designs, plans, and develops clinical evaluation research studies.
- Prepares and authors protocols and patient record forms.
Other
- Requires a Baccalaureate degree
- Minimum of 4 years of relevant experience, or an advanced degree with a minimum of 2 years of relevant experience.
- Strong communication skills
- Minimum of 4 days a week onsite
