Hays is collaborating with an international pharmaceutical company specialized in the development, manufacturing, and commercialization of medicines , with a strong focus on generics and a solid commitment to R&D and clinical development . The project focuses on the review and validation of clinical and bioanalytical documentation within the Clinical Development area, in close collaboration with CROs and internal teams such as Quality and Pharmacovigilance. The team is currently in an active phase reviewing multiple clinical studies, with potential continuity depending on upcoming regulatory needs. We are currently looking for a Medical Writer – Clinical Development (Freelance) to support this project, working closely with the clinical team and external partners. Key Responsibilities
- Review clinical and bioanalytical documentation , including Clinical Study Reports (CSRs) , PK/BE reports, and related materials
- Assess bioanalytical reports in compliance with ICH M10 gu...