TRABAJO REGULATORY AFFAIRS MEDICAL DEVICES BARCELONA, BARCELONA

Position: regulatory affairs management director (rad), regulatory science & execution, global regulatory affairs location: barcelona - spain (3 days working from...

Documentation preparation: prepare comprehensive regulatory documentation for medical devices, including ivds and medical device software, ensuring compliance with...

Run regulatory local projects meeting timelines and costs understand relevant legislative and regulatory guidance applicable to activities prepare risk benefit analysis...

The new assets medical advisor will report to the medical director... position summary the new assets medical advisor is an office-based position within spain &...

Rwe medical lead grade: l3... represent global rwe in country medical leadership team to facilitate seamless communication, coordinate and alignment of rwe with...

Lead and contribute to medical monitoring of trials provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities...

Support az compliance with medical device, device constituent and digital health regulatory and legal requirements, including implementation of new regulatory &...

Back up of the flu medical lead/head in global/local meetings... job title:  medical advisor flu/covid spaiin location:  barcelona (preferred) alternative: madrid...

• collaborate with key stakeholders, including medical affairs and other partner functions... • ensure that the medical content developed aligns with mc&i priorities...

Our state-of-the-art, dog-friendly campus includes a medical center, canteen, and collaborative spaces for networking and relaxation...    join nestlé #beaforceforgood ...

Pharmacovigilance), clinical research, or regulatory affairs solid knowledge in drug safety related processes (incl... the medical safety and processes manager will...

Broad background of experience working in pharmaceutical business and prior experience in several areas within regulatory affairs...   participate in cross-functional...

Prepare regulatory documentation and design processes with the quality and regulatory affairs teams to comply with the artificial intelligence regulation and other...

Experience in all study phases and in rare medical conditions preferred... good medical knowledge and ability to learn relevant alexion therapeutic areas...

Strong understanding of regulatory requirements and guidelines for clinical trials, including ich-gcp and local regulatory requirements... in addition to your competitive...

Prepare and manage regulatory submissions... analyze data from devices to improve performance... knowledge of clinical trial methodologies and regulatory processes...