Senior Clinical Research Specialist
$55,200–$82,800 year
On-siteMaastricht, Limburg, The Netherlands or Trévoux, Auvergne-Rhône-Alpes, France
Job Summary
Design, plan, and oversee international pre-market and post-market clinical studies for Core Surgical Innovations. Prepare and author clinical study protocols, patient follow-up forms, and related documentation while managing operational aspects of trials in collaboration with cross-functional teams. Conduct registered and non-registered clinical studies to generate robust evidence supporting safety, efficacy, and economic value for global regulatory approvals and reimbursement. Interpret investigation results to support new medical device applications and manage clinical supply operations, site selection, and vendor management. Ensure full compliance with Good Clinical Practice and applicable country-specific regulations while representing Medtronic in local evidence dissemination and stakeholder partnerships.
Required Qualifications
- Bachelor's degree in Life Sciences, Clinical Research, Nursing, Biomedical Sciences, or a related field
- Minimum of 4 years of relevant experience in a similar role within a manufacturing environment
- Advanced knowledge of the field, typically gained through a combination of higher education and professional experience
- Fluency in English, both written and spoken
- Experience working with a Clinical Trial Management System (CTMS)
- Strong project management, communication, and problem-solving skills
- Investigational Device Exemption (IDE) study experience and experience with investigational device accountability, tracking, and reconciliation
- In addition, Medtronic will provide reasonable accommodations for qualified individuals with disabilities
Desired Qualifications
- For the France-based role, fluency in French, both written and spoken, is also required
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