Sr Clinical Research Spec
Core
Lead post-market clinical research and medical affairs activities to generate and disseminate evidence for Medtronic's marketed devices, bridging unmet medical needs with clinical insights.
Role type
Senior Clinical Research Specialist (Medical Affairs)
Builds
Clinical evidence, strategic medical plans, and insights for cardiovascular and vascular device portfolios.
Domain
Healthcare / Medical Devices / Cardiovascular
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Post-market clinical research planning, project management, KOL/stakeholder management, GCP/GPSP regulatory knowledge, English business communication, literature review, statistical analysis basics, medical/scientific information synthesis
Preferred skills
PCI/cardiovascular surgery/peripheral vascular/TAVR/TPVI domain experience, PMDA consultation experience, ISO 14155 knowledge, Real World Evidence analysis, medical strategy planning
Technologies
GCP, GPSP, ISO 14155
Responsibilities
Plan and execute post-market surveillance (PMS) and post-market clinical research (PMR); manage investigator-initiated studies (ERP/ISR) including site contracts and progress tracking; develop and implement evidence generation plans based on marketing and medical strategies; identify unmet medical needs and evidence gaps; promote evidence dissemination via conferences and publications; support advisory board operations; build relationships with domestic and international stakeholders.
Seniority
Senior, hands-on IC
