TRABAJO REGULATORY AFFAIRS MEDICAL DEVICE BARCELONA, BARCELONA

Veeva) medical information / medical communication experience globally... this is what you will do: the director, strategic operations lead, medical information...

Communication with regulatory authorities... knowledge of medical device legislation (mdr, mdcg, iso10993, iso 13485, iso 14155 etc)english proficiency, capability...

Strong scientific and/or dermo cosmetics & medical device knowledge... experience in medical writing & medico marketing... we are looking for a medical affairs/...

The metabolics medical advisor will report to the medical affairs manager, metabolics... educate the  medical community with up-to-date medical and scientific...

The global development medical director plays a critical role in the medical monitoring of a clinical study ensuring safety to patients... safety or efficacy)...

• demonstrates medical leadership by contributing to key medical and scientific events, advisory boards, and rwe generation... job description:the medical science...

The senior global development medical director plays a critical role in the medical monitoring of a clinical study ensuring safety to patients...

You will provide expert medical input into the preparation of regulatory documents and interactions with regulatory authorities... you will lead and contribute to...

The clinical research medical advisor is a global clinical development role with medical responsibility for the clinical trial process...

• collaborate efficiently on clinical safety tasks with colleagues from clinical development, regulatory affairs, medical affairs, medical information, statistics...

At least 1 year of medical affairs or msl experience... the medical scientific liaison (msl) role is a position specifically designed to meet the needs of scientific...

Location: barcelona, spain (on-site) the associate director, patient safety device & digital contributes to the patient safety in-vitro diagnostic device process...

Specialized focus on digital regulatory science, clinical medical affairs, pv (pharmacovigilance), sustainability, and other science-related project activities...

Drug supply, contracting, regulatory documentation, publication review etc... the edd will work hand in hand with the scientific study leader who is responsible...

Contributes to the development of medical oversight plan (mop), study level safety reviews and study-level medical monitoring activities... oncology research & development...

Provide expert scientific input into the preparation of regulatory documents and interactions with regulatory authorities... support and contribute to medical monitoring...

medical devices)... experience in developing multidisciplinary medical device is a plus... preferred to have detailed understanding of active implantable medical...