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 .

Aumente sus posibilidades de llegar a la fase de entrevista leyendo la descripción completa del puesto y enviando su solicitud sin demora.

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...