Location: Athens (office based)

Your New Role

The Study Start-Up Specialist is responsible for the end-to-end execution of clinical trial start-up activities and regulatory submissions at country and site level. The role ensures timely study activation, regulatory compliance, and delivery of key start-up milestones through effective collaboration with internal teams, investigators, Ethics Committees, Health Authorities, and external partners.

The role requires professionals with:

• Strong knowledge of clinical trial regulations, submission requirements, and ICH-GCP.
• Experience managing clinical trial submissions and study start-up activities.
• Digital & AI curiosity, proficiency with clinical trial management systems, eTMF platforms.
• Strong project management, planning, organizational, and prioritization skills.
• Excellent analytical thinking, problem-solving a...