FSP Clinical Trial Coordinator Finland
Core
Administrative and technical support for clinical trial site activation, feasibility assessments, and regulatory compliance within the pharmaceutical/biotech industry.
Role type
Clinical Trial Coordinator II (Local/Central)
Builds
Site activation critical paths, feasibility assessments, regulatory compliance packages, and study documentation.
Domain
Clinical Trials / Pharmaceutical Operations
Required skills
Site activation coordination, feasibility assessment, regulatory document review, (e)TMF management, site list development, vendor tracking, study metrics analysis, SOP compliance, stakeholder liaison
Preferred skills
Local market knowledge, site tiering expertise, training new personnel, strategic feasibility process development
Technologies
(e)TMF, CTMS, Activate, eTMF, RBM systems
Responsibilities
Coordinate assigned trial activities per task matrix; perform file reviews (department, internal, country, investigator); process documents and manage (e)TMF; develop and review site lists for feasibility; conduct feasibility visits and phone interviews with site personnel; maintain vendor trackers and study metrics; support regulatory submissions and compliance reviews; train new staff on processes and systems.
Seniority
Mid-level, hands-on IC
