You will be responsible for executing global study start-up activities to ensure timely trial document and task completion to enable country health authority and ethics committee submissions and site activation to meet ambitious recruitment plans
Job Summary
You will be responsible for executing global study start-up activities to ensure timely trial document and task completion to enable country health authority and ethics committee submissions and site activation to meet ambitious recruitment plans.
ICON offers a range of competitive benefits focused on well-being and work-life balance, including health insurance, retirement planning, and a global employee assistance program.
ICON is committed to providing an inclusive and accessible environment for all candidates and promotes a workplace free of discrimination and harassment.
Matching Summary
You will be responsible for executing global study start-up activities to ensure timely trial document and task completion to enable country health authority and ethics committee submissions and site activation to meet ambitious recruitment plans.
Skills & Requirements
Must-have
Global study start-up leadership
Clinical Trial Management System (CTMS)
Trial Master File (TMF) inspection readiness
Vendor and site activation coordination
Health Authority and Ethics Committee submissions
Protocol and ICF template management
Nice-to-have
Team leadership and planning
Experience in pharmaceutical industry
Working within inclusive and diverse culture
Remote work flexibility
Experience with investigator grant plans
Key Requirements
Right to work in UK, Spain, Poland or Bulgaria
Relevant senior study start-up experience
Experience in Clinical Research, Biotech or Pharmaceutical industry
Availability to start in May 2026
Work Rights
Must have right to work in UK, Spain, Poland or Bulgaria