Job Description:
Job Title: Clinical Trial Documentation Specialist
Location: Florence, Italy
Industry: Biotechnology & Life Sciences
Job Description:
We are looking for a motivated and skilled Clinical Trial Documentation Specialist to join our team in Florence, Italy under the Biotechnology & Life Sciences sector. In this role, you will be responsible for managing and organizing documentation for clinical research projects in compliance with regulatory and GCP requirements. The ideal candidate should have experience in clinical trial support and document control. Key duties include preparing trial master files (TMF), ensuring version control, maintaining audit readiness, and supporting investigators and CROs with essential documentation. You will also assist with ethics submissions and monitor site-level record keeping. This role requires thoroughness, regulatory understanding, and excellent documentation practices. It is a key role in ensuring research transparency and compliance in Florence.
Job Requirement:
We are seeking a capable and enthusiastic individual for the role of Clinical Trial Documentation Specialist in Florence, Italy under the Biotechnology & Life Sciences sector. The ideal candidate should demonstrate document management experience in clinical research. Key requirements include:
• Familiarity with ICH-GCP guidelines and clinical trial documentation requirements
• Experience using electronic document management systems (EDMS)
• Attention to detail and ability to manage sensitive documents
• Effective communication with research teams and ethics boards
• Background in life sciences, health administration, or clinical research coordination
This role suits individuals committed to upholding data integrity and compliance in research. We invite candidates ready to strengthen clinical documentation standards in Florence.
