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. We are currently looking for a Medical Writer – Clinical Development (Freelance) to support this project, working closely with the clinical team and external partners. Ensure consistency across clinical, statistical, and bioanalytical data
- Perform quality control (QC) of documentation: PK data, adverse event reporting, and overall consistency
- Liaise with CROs for document review and validation
- Clinical Development, QA, and Pharmacovigilance
- Considerable experience as a Medical Writer in a clinical research environment
- Advanced level of English Contract opportunity through Hays, working with an international pharmaceutical company
- Part-time project (approximately 3 full days per week)
- Possibility of 100% remote work
- Close collaboration with the Clinical Development team
- Initial duration of 4 months (likely to extend) with immediate start