See all jobs on JobTailor
Search thousands of fresh jobs every day.
- Fresh listings
- Fast filters
- No subscription required
Senior Clinical Research Specialist
MedtronicSenior Clinical Research Specialist in charge of international pre-market and post-market clinical studies at Medtronic. Responsible for high-quality study results supporting strategic objectives in healthcare technology.
Core Competencies
Role fitUse this summary to align your resume positioning with the role.
Demonstrates expertise in designing and overseeing clinical evaluation and research studies, with a strong focus on compliance with Good Clinical Practice (GCP) and regulatory requirements. Proficient in managing clinical trials, including budget preparation and vendor selection, while effectively communicating with cross-functional teams and external partners.
ATS Keywords
Tailor your resumeTip: use these terms in your resume and cover letter to boost ATS matches.
Tech Stack
Tools & technologiesAbout the role
Key responsibilities & impact- Design, plan, and oversee clinical evaluation and research studies
- Prepare and write clinical study protocols, patient tracking forms, and related study documents
- Conduct registered and unregistered clinical studies for products addressing unmet medical needs and/or demonstrating commercial potential
- Oversee and interpret clinical investigation results to support new submissions for medical devices, drugs, or consumer healthcare products
- Manage and resolve operational aspects of clinical trials in collaboration with cross-functional project teams, ensuring compliance with standard operating procedures, Good Clinical Practice (GCP), and applicable country-specific regulations
- Support clinical trial planning activities, including budget preparation, clinical procurement operations, and site and vendor selection where needed
- Represent Medtronic from a clinical research perspective within the country or region, building effective internal and external partnerships, collecting feedback from customers and local authorities, and leading local evidence dissemination and outreach efforts.
Requirements
What you’ll need- 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 domain knowledge, typically acquired through a combination of higher education and professional experience
- Proficiency in English, both written and spoken; for the France-based position, proficiency in French, both written and spoken, is also required
- Experience working with a Clinical Trial Management System (CTMS)
- Strong project management, communication, and problem-solving skills
- Investigational Device Exemption (IDE) experience and experience with accountability, tracking, and reconciliation of investigational devices preferred.
Benefits
Comp & perks- Competitive and flexible salary
- Commitment to our employees
- Wide range of benefits, resources, and competitive compensation plans