FSP_Clinical Trial Coordinator (Sponsor: Roche)
Core
Administrative and technical support for clinical trial site activation, feasibility assessments, and audit readiness within the global medical research community.
Role type
Clinical Operations Delivery Associate II (Clinical Trial Coordinator)
Builds
Site activation critical paths, feasibility assessments, and regulatory compliance packages for clinical trials.
Domain
Healthcare / Clinical Research
Required skills
Site activation coordination, feasibility assessment, regulatory document review, (e)TMF management, site list development, data analysis, stakeholder communication, SOP compliance, training support
Preferred skills
Bachelor's degree, 2+ years of relevant experience, local market knowledge, system support capabilities
Technologies
MS Office (Word, Excel, PowerPoint), clinical trial database systems, Activate & eTMF, CTMS
Responsibilities
Coordinate and oversee assigned trial activities per task matrix; perform file reviews (department, internal, country, investigator); process documents for (e)TMF; conduct on-site feasibility visits; train new personnel; maintain vendor trackers and study metrics; support regulatory submissions and compliance reviews; develop and maintain site lists and contact details.
Seniority
Mid-level, hands-on IC
