Regulatory Medical Writer

OverviewSenior Medical Writer role at Azur Health Science. If you are looking for a position in a growing company where you can join the role as a Senior Medical Writer working on projects that make tangible differences in the lives of patients with rare disease, keep reading!RoleAzur Health Science are looking for a dynamic and autonomous Senior Medical...

A healthcare-focused organization is seeking a Senior Medical Writer to contribute to meaningful projects in the rare disease sector. This role involves preparing regulatory documents, mentoring junior writers, and interacting with client teams. Candidates should have strong leadership skills and a minimum of 3 years in regulatory writing. Opportunities for...

Hemerion Therapeutics is seeking a skilled Technical Product Manager to own the full lifecycle of our medical devices, from design through production and post‑market surveillance, including hands‑on lab work.The role requires a minimum of 10 years in medical device development, deep regulatory expertise (CE/FDA), and fluency in English. Collaboration...

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for a Manager, Regulatory Affairs based in France. This role offers the opportunity to lead regulatory affairs activities across multiple international markets within a dynamic clinical research environment. You will oversee regulatory...

ixolabs.ai is seeking contributors to write original medical questions that require synthesis and clinical reasoning. You will verify answers against primary research or guidelines, document rationale and citations, and refine cases with ambiguous or simple responses. Strong written English and biomedical expertise are preferred for accurate, credible...

Jobgether, on behalf of a partner company, is seeking an Associate Director, Medical Affairs based in France. You will lead scientific engagements, publications, and external communications while shaping Medical Affairs strategy across the product lifecycle.This remote role includes travel for congresses and engagements. You will develop KTL plans, provide...

Write original medical questions that require synthesis and clinical reasoning. Verify answers against primary research or authoritative guidelines, document the rationale and citations, test model responses and revise cases that are ambiguous or too simple.Professional backgroundPreferred contributors are medical students, residents,

This position is listed on behalf of a partner company, who manages all applications and next steps. Our partner is looking for an Associate Director, Medical Affairs based in France. As Associate Director, Medical Affairs, you will serve as a scientific leader and subject-matter expert across a broad range of Medical Affairs activities. You will...

IXO is engaging specialists to evaluate biomedical-engineering judgments that connect device design to verification evidence. Your contribution is technical work: make the reasoning inspectable, identify substantive errors and provide evidence that supports a reliable assessment.Work you will doAssess medical-device designs and