Regulatory Jobs
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Global Regulatory Lead
Title: Associate Director Regulatory AffairsA small but growing clinical stage company is seeking an Associate Director Regulatory Affairs to join the team in a remote capacity. They are seeking a well-rounded RA professional to lead the Regulatory Strategy for their pipeline of phase III products in the rare disease space. Responsibilites:Serves a...
Senior Manager of Regulatory Affairs
Title: Regulatory Affairs Senior Manager Summary: Our client is seeking an experienced Senior Manager of Regulatory Affairs to lead the preparation and submission of global regulatory filings, ensuring compliance with clinical, pre-, and post-market requirements. This role involves cross-functional collaboration, regulatory strategy development, an...
Director, Medical Writing *On-site in NYC*
Director, Medical WritingA leading, global biopharmaceutical company is seeking a highly skilled Director of Medical Writing. This role is pivotal in the Clinical Development function, and will lead the execution of regulatory and clinical documents. Responsibilities:Develop a range of regulatory and clinical documents, including clinical protocols...
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Senior Director Regulatory Advertising & Promotion
Title: Senior Director Regulatory Advertising & Promotion A pioneering biopharma is looking to grow the legal team with a Senior Director Regulatory Advertising & Promotion to support their new product launch. This will be a hands-on position, serving as a high level operational and strategic lead in complying with regulatory guidelines. This perso...
Project Engineer, Medical
EPM is collaborating with a leading medical device company in the USA to find a skilled Engineer specializing in the evaluation and testing of medical electrical devices. This role is crucial in ensuring products meet regulatory standards and industry requirements.Role OverviewThe Engineer will be responsible for conducting assessments and tests on...
Regulatory Affairs Specialist
We have a current opportunity for a Regulatory Affairs Specialist on a contract basis. The Regulatory Affairs Consultant will be responsible for providing strategic guidance on regulatory requirements and submissions for medical devices. This role involves ensuring compliance with global regulations, preparing and managing regulatory submissions, a...