TRABAJO RESPONSABLE REGULATORY AFFAIRS MEDICAL MADRID, MADRID

Dossiers), and oversee compliance with regulatory materials... proven ability to review translations, manage regulatory submissions (e... collaborate with cross-functional...

Join us as a medical affairs trainee... medical science liaisons - msls)... role purpose the medical affairs trainee will provide comprehensive support to medical...

Directs the operational function in medical affairs to achieve organizational objectives taking key decisions during the conduct... overall purpose of job responsible...

Job description job function:                                                    the medical education specialist is responsible for the operational management and...

Clinical research director (crd), global feasibility lead (gfl), ta early planning leads, global project team, pharmacovigilance, and regulatory affairs...

medical writing on-call responsibilities on an as assigned basis... preferred qualifications: education:  mpharma, pharmad experience and/or training: call center...

Who are you? we are looking for a talented professional with medical writing, scientific writing skills, who can work on developing medical and promotional content...

Experiencia previa de almenos 2 años en regulatory affairs o evaluación toxicológica en el sector cosmético preferiblemente...   tus principales responsabilidades:...

Facilitate medical and scientific field intelligence – for example, competitor research and medical strategies, educational activities – and communicate, where...

Facilitates regulatory submissions and communications by communicating with regulatory affairs during the submission process... experience with medical device clinical...

G pv, regulatory affairs activities... a) for wholesale distribution of medicinal product and medical devices... report monthly to local competent authority the...

We’re always looking towards the future, anticipating changes in medical science and technology... food and drug administration (fda) and local regulations, other...

The ideal candidate will bring international experience, preferably from a medical device or healthcare company, or a law firm’s healthcare team...

Services overview: local trial management services provides local management of a clinical trial (or medical affairs data generation activity) in a country or countries...

The project manager is responsible for maintaining the proper project documentation and ensuring compliance with sops and regulatory requirements for clinical...

Establishes and maintains excellent working relationships with external stakeholders, in particular investigators, study trial coordinators and other site staff...