Clinical Regulatory Affairs Specialist

Our team members are at the heart of everything we do. At Cencora, we are united in our responsibility to create healthier futures, and every person here is essential to us being able to deliver on that purpose. If you want to make a difference at the center of health, come join our innovative company and help us improve the lives of people and animals...

Ergomed Group in Australia seeks a Specialist, Local RA & PV Network to act as local country person responsible for pharmacovigilance and regulatory affairs, ensuring compliance with national requirements and supporting MAH lifecycle.You will lead PV/RA activities at local level, coordinate with MAH and authorities, screen for regulatory intelligence, manage...

Worldwide Clinical Trials is seeking an experienced Regulatory Affairs professional to lead submissions across EMEA, APAC and LATAM. You will provide expert regulatory guidance, coordinate with ethics committees, and support clinical start-up activities.The role requires a strong background in ICH GCP, cross-cultural communication, and fluency in English;...

We are looking for a Regulatory Affairs / Clinical Affairs Specialist with strong experience in pharmaceuticals and medical devices. Manage regulatory projects in pharmaceuticals and medical devices Advise clients on regulatory compliance, product registration, and market access Prepare and submit regulatory dossiers to competent authorities Monitor...

Who We AreWe’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.Why WorldwideWe believe everyone plays an important...

IQVIA in Paris is seeking a Senior Regulatory Affairs Specialist to lead regulatory activities for medicinal products and lifecycle management, ensuring compliance across the portfolio.You will prepare and submit documentation, act as the primary regulatory contact with Health Authorities, review labeling and artwork, and collaborate with Medical Affairs,...

En Carta Diagnostics is a synthetic biology diagnostic company focused on the development, manufacturing, and commercialization of innovative point-of-need diagnostic devices addressing major unmet medical needs.Our vision: Transforming every smartphone on the planet into a PCR machine, to bring diagnostics for better care, everywhere.Our flagship product,...

🔎 Title: Senior Regulatory Affairs Consultant🔸 The CompanyIf you are a QA/RA professional with an interest in innovation and groundbreaking development, we have an incredible role for you. This is a chance to join an established midsize Software as a Medical Device company.🔹 As a Regulatory Affairs Consultant your mission is to:Develop and execute...

En Carta Diagnostics in Paris is seeking a Senior Regulatory & Clinical Affairs Manager to own regulatory and clinical strategy for IVDR and FDA pathways, guiding products from technical file to market authorization.You will lead cross‑functional teams across biology, engineering and quality, build robust regulatory routes, and ensure timely, compliant...