Senior CTA Regulatory or Finance in Türkiye

• Support contract management, including tracking negotiations, maintaining templates, and ensuring compliance
• Maintain study trackers, clinical trial systems (e.g., CTMS), and reporting tools
• Support financial activities, including payment calculations and adherence to financial procedures
• Assist with regulatory submissions (IRB/ERC, authorities) and preparation of submission packages
• Coordinate, prepare, and manage study documentation and correspondence
• Ensure proper handling, distribution, and archiving of essential clinical trial documents
• Support eTMF activities, including reconciliation and quality control
• Collaborate with sites by collecting and tracking required documents for study start-up and conduct

Experience:

• University or college degree (biological or life science preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing licensure, medical or laboratory technology).
• Understanding of ICH-GCP guidelines and of the clinical trial process.
• A minimum of 2 years of industry experience in a related role (e.g., IHCRA, CTA, study coordinator).
• Fluent in English