Senior Medical Writer M - F H/F

Description

Les missions du poste Biotrial, prestataire de service de l'industrie pharmaceutique, accompagne ses clients dans toutes les étapes du développement des médicaments et dispositifs médicaux depuis plus de 35 ans. Biotrial est leader en développement précoce, acteur incontournable dans les secteurs les plus scientifiques et innovants de la pharmacologie non clinique, des essais cliniques, de l'oncologie, de la bioanalyse et du traitement des données. With over 35 years of expertise, Biotrial, a contract research organisation, helps to safeguard and improve the health of millions of people by advancing the treatment of diseases. By joining our company at one of our sites in Europe or the Americas, you will become part of a highly effective organisation and team. Teamwork and cross-departmental cooperation enable us to offer cutting-edge services. You will therefore be required to work closely with various departments. As part of our expansion, we are currently seeking a Senior Medical Writer (M/F) for a permanent contract, based in Rennes. Your role as Senior Medical Writer will enable you to apply your expertise in drafting deliverables related to clinical and non-clinical studies. The role is open to candidates working 100% remotely. Your main responsibilities in this role will include: - Drafting documents in the following areas: Clinical: Drafting clinical study protocols, clinical study reports (Phases I to IV), and other deliverables (such as DSURs, Investigator Brochures, CTDs) across various therapeutic areas (Phase I safety studies, oncology, neurology, cardiovascular, etc.) Non-clinical: non-clinical reports - Carrying out quality control of clinical study protocols, clinical study reports and other deliverables - Writing scientific manuscripts and abstracts - Preparing training materials - Helping to develop and optimise our procedures and document templates - Working closely with various departments (statistics, quality assurance, etc.) - Taking part in com