Medtronic is looking to solve healthcare access and equity for all by breaking down barriers to innovation in a more connected, compassionate world.
Requirements
- Knowledge of/experience with CTMS/EDC/TMF
- Experience with Good Clinical Practice (GCP)
- Clinical experience
- Site Management experience (site or sponsor)
- Bachelor's degree in degree in engineering, life sciences, or related medical/scientific field
- Experience with clinical trials and scientific projects
- Ability to work with various internal and external parties
Responsibilities
- Oversees, designs, plans and develops clinical evaluation research studies.
- Prepares and authors protocols and patient record forms.
- Conducts registered and non-registered clinical studies of products that have been determined to satisfy a medical need and/or offer a commercial potential.
- Oversees and interpret results of clinical investigations in preparation for new drug device or consumer application.
- 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 respective within the country / region and also collects feedback from local customers and authorities.
Other
- Bachelor's degree plus 2+ years of related experience
- Ability to work a minimum of 4 days a week onsite
- Ability to interact with a computer, and communicate with peers and co-workers
- Ability to be independently mobile
- Travel requirements not specified
