Senior Specialist, Clinical Research Monitoring
Core
Monitoring clinical trials for medical devices and pharmaceuticals, ensuring compliance and data integrity from trial initiation to closure.
Role type
Senior Specialist, Clinical Research Monitoring
Builds
Clinical trial data and regulatory compliance for medical device and pharmaceutical products
Domain
Healthcare / Clinical Research / Medical Devices & Pharmaceuticals
Deliverable
production ML models | product features | dashboards & analysis | research | client delivery | infrastructure | physical/clinical work
Required skills
Clinical trial monitoring, Site selection and contracting, IRB management, Case report form review, Source data verification (SDV), Adverse event reporting, Regulatory knowledge
Preferred skills
International clinical trial experience, English reading and writing proficiency
Responsibilities
Oversee clinical trial execution from start to finish, including site selection, contract negotiation, and regulatory submissions
Seniority
Senior, hands-on IC
