Senior Study Start Up Associate
Core
Lead site start-up and activation tasks, including feasibility assessments, site identification, contract negotiation, and regulatory submissions to ensure study initiation quality and compliance.
Role type
Senior Study Start Up Associate
Builds
Clinical study sites and activation plans
Domain
Healthcare / Clinical Research
Required skills
Site identification, contract negotiation, regulatory compliance, feasibility assessment, patient safety documentation, Master and Country Specific Subject Information Sheets, Informed Consent Forms
Preferred skills
Medical/science background, independent work, guiding others
Technologies
None stated
Responsibilities
Conduct feasibility assessments, identify sites, negotiate site contracts, prepare regulatory and ethics submissions, develop and review patient information sheets and consent forms
Seniority
Senior, hands-on IC
