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/...