REGULATORY MEDICAL AFFAIRS REGULATORY jobs in SAN DIEGO CA, United Kingdom

commercialized products. The Oncology Medical Director - MRD is a member of the Medical Affairs team and is both a leader... development, pathology and clinical lab operations, biostatistics, clinical affairs, regulatory, market access, and commercial...

of strong Regulatory Affairs experience in the medical device industry. Proven prior experience required owning and managing the end...Job Description Summary As Staff Regulatory Affairs Specialist, Infusion, you will be responsible for Regulatory...

, compile and publish electronic post-market regulatory submissions. Compile Technical Documentation for IVD medical devices... sciences or engineering with a minimum of 5-8 years direct experience in Regulatory Affairs within an IVD or Drug/Biologics...

agencies. Represents the Regulatory Affairs department as a member of project teams, certain boards, and as part... of other meetings as the need arises. YOU’RE AWESOME AT: Provides regulatory affairs support for all aspects of product development...

Affairs Specialist to our team. The Senior Regulatory Affairs Specialist leads regulatory compliance objectives for the...+ years of experience, ideally in a Regulatory department (medical device or pharmaceutical). An equivalent combination...

search of an accomplished and dynamic Senior Director of Regulatory Affairs to join our team. This pivotal role... and independent consultants, as required. Qualifications: Minimum of 10 years of experience in Clinical Regulatory Affairs...

, pharmaceuticals, or medical devices. A relevant bachelor's degree and prior experience in FDA compliance or regulatory affairs...Position Overview: The FDA Compliance & Regulatory Specialist is responsible for ensuring the company's compliance...

of which a minimum of 6 years must be Regulatory Affairs experience in drug development at a research-based pharmaceutical company, including... regulatory department with process development/improvement activities to support organizational optimization and more consistent...

’s degree or equivalent in a life science and 8+ years of experience in regulatory affairs in the pharmaceutical/biotech... and execution of regulatory CMC plans for assigned development and commercial projects leading to successful preparation...

. Job Description We are seeking a highly motivated and experienced Regulatory Specialist to join our Regulatory Affairs team. The ideal candidate... the company’s products. Requirements · Bachelor’s degree in Life Sciences, Biotechnology, Regulatory Affairs...

legislations, and regulatory governance Experience building medical affairs mission and functionality in a drug, medical device..., you will do more and become more than you ever thought possible. Position Summary: Illumina’s VP, Medical & Clinical Affairs will be responsible...

your talents. Executive Director, Clinical and Medical Affairs Welcome to an inspired career. At Halozyme, we are reinventing... Director, Clinical and Medical Affairs, reporting to our Chief Medical Officer (CMO), leads all related activities for assigned...

stakeholders, including regulatory, product development, marketing, and scientific affairs, to ensure the studies are designed... for today’s connected consumers! JOB SUMMARY Truvian is looking for a Director/Sr. Director, Clinical Development/Clinical Affairs...

. Consistently execute upon the current Medical Affairs strategy and MSL priorities Respond to unsolicited research/clinical... Medical Affairs teams, clinical operations, sales, and marketing teams Demonstrate strong scientific acumen through self...

execute upon the current Medical Affairs strategy and MSL priorities Respond to unsolicited research/clinical inquiries... with internal stakeholders including but not limited to MSL field partners, R&D, US as well as Global Medical Affairs teams...

&D Medical Affairs in writing scientific communication documents such as manuscripts, abstracts, and podium presentations...Job Title Senior Medical Writer Job Description As the Senior Medical Writer, you will be responsible for authoring...

recruitment, training and development of the clinical teams Identify and select clinical consultants Work with Medical Affairs... project managers, preclinical/clinical pharmacology, biometrics, regulatory, drug safety). May work closely with Research...