Clinical Trial Coordinator - FSP - UK
Core
Administrative and technical support for clinical trial site activation, feasibility assessments, and regulatory compliance within pharmaceutical/biotech projects.
Role type
Clinical Trial Coordinator II (Clinical Operations)
Builds
Site activation critical paths, feasibility assessments, regulatory compliance packages, and study documentation.
Domain
Clinical Trials / Pharmaceutical Services
Required skills
Site activation coordination, feasibility assessment, regulatory document review, (e)TMF management, site list development, vendor management, finance support (Pos, invoicing, budget tracking), system administration (CERPS, Ariba, Fiori, Veeva Payments), data analysis, stakeholder communication.
Preferred skills
Bachelor's degree, 2+ years of relevant experience, knowledge of clinical trial SOPs and regulatory guidelines.
Technologies
CERPS, Ariba, Fiori, Veeva Payments, CTMS, (e)TMF
Responsibilities
Coordinate assigned trial activities per task matrix; perform file reviews (department, internal, country, investigator); process documents for (e)TMF; develop and review site lists for feasibility; conduct feasibility visits (Asia Pac); support regulatory submissions and compliance reviews; manage vendor trackers and finance tasks; train new personnel; maintain study metrics and databases.
Seniority
Mid-level, hands-on IC
