Publicada el 16 junio
Misión del puesto
Hays
Si los siguientes requisitos del puesto y la experiencia coinciden con sus habilidades, por favor, asegúrese de enviar su solicitud sin demora.
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 xhfqzwm 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
Hay opciones de teletrabajo/trabajo desde casa disponibles para este puesto.