Remote Medical Writer for EU MDR CE Submissions

Glyance is a small and growing medical aesthetics company developing and manufacturing high-quality dermal fillers. We operate strictly under ISO 13485 and are preparing for CE certification. As a lean organization, we are looking for a hands-on contract Medical Writer who is comfortable working in a small team and taking real ownership of our CE submission...

Syneos Health is seeking a Principal I/II Medical Writer (Clinical / Submissions exp) for fully remote work across Europe (Italy, UK, Spain, Poland or Ireland). The role focuses on regulatory submissions, medical writing deliverables, and collaborative partnership with clinical teams to accelerate drug development and regulatory success. You will work within...

Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. Updated: Today Location: Remote, MI, Italy Job ID: -OTHLOC-3531-2DR Description Single sponsor Principal I/II Medical Writer (Clinical / Submissions exp) fully remote in Italy, UK, Spain, Poland or Ireland. Syneos Health® is a...

Work Schedule Standard (Mon-Fri) Environmental Conditions Office Job Description At Thermo Fisher Scientific, you will discover meaningful work that makes a positive impact on a global scale. Join our colleagues in bringing our Mission to life - enabling our customers to make the world healthier, cleaner, and safer. We provide our teams with the...

Mira is a San Francisco-based hormonal health company providing integrative care and hormonal testing for over 300,000 customers. In 2023, we were recognized by Inc. 5000 as America's fastest-growing femtech company. Mira’s breakthrough innovation was creating the market’s only FDA-compliant at-home hormone monitor with quantitative testing technology....

Overview In this Regulatory Affairs Lead role, you shape IVD regulatory strategies, guiding performance evaluation and marketing authorizations. You will act as the regulatory lead for global project teams, coordinating interactions with authorities and ensuring compliant submissions. The role supports lifecycle management and continuous improvement within...

Parexel International is seeking an experienced Regulatory Affairs professional to lead regulatory strategy for medical devices and combination products across Europe.You will guide clinical investigations, CE markings, and interactions with health authorities, advising global project teams throughout development and authorization processes.We value deep EU...

Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Tests, in order to expand the RA Team, is looking for a: Senior Regulatory Affairs Specialist FDA & International Registrations Key Responsibilities: * Define and implement regulatory strategies to...

Sentinel Diagnostics, leader in the Development and Production of Diagnostic Kits for Clinical Chemistry, Immunology, Molecular Biology, Chromatography and Rapid Tests, in order to expand the RA Team, is looking for a:Senior Regulatory Affairs Specialist FDA & International RegistrationsKey Responsibilities:Define and implement regulatory strategies to...