Available Jobs
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Associate Director Regulatory Affairs |
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Location: London Area Recruiter: Pharma Partners Recruitment Job Hours: Full-time |
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| Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical developm... | ||||
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Associate Director Regulatory Affairs |
Apply | |||
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Location: London Area Recruiter: Pharma Partners Recruitment Job Hours: Full-time |
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| Job title: Associate Director, Regulatory Affairs A Pharmaceutical business in London is looking for an Associate Director, Regulatory Affairs to join their Global team. In this role you will provide strategic regulatory and scientific assessment on preclinical requirements, and clinical developm... | ||||
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Associate Director Regulatory Affairs CMC |
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Location: United Kingdom Recruiter: Wax Job Hours: Full-time |
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| Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team. This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creativ... | ||||
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Associate Director Regulatory Affairs CMC |
Apply | |||
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Location: United Kingdom Recruiter: Wax Job Hours: Full-time |
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| Our client, a successful and growing Biotechnology organisation, is looking to hire a new addition to the Regulatory CMC team. This role is responsible for preparing regulatory CMC submission strategy for rare disease drugs (both biologics and small molecules) and an opportunity to design creativ... | ||||
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Regulatory Affairs & Clinical Docs Senior Associate |
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Location: Manchester Recruiter: Carrot Recruitment Job Hours: Full-time |
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| The Role Completing regulatory dossiers for global submissions, including 510(k) applications Maintain existing products, ensuring compliance Complete and update clinical documents including Clinical Evaluation Plans (CEP) and Clinical Evaluation Reports (CERs) Assist with both... | ||||
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Global Regulatory Affairs, Associate Director (Oncology) |
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Location: Cambridge Recruiter: Gilead Sciences Job Hours: Full-time |
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| Job Description At Gilead, we’re creating a healthier world for all people. For more than 35 years, we’ve tackled diseases such as HIV, viral hepatitis, COVID-19 and cancer – working relentlessly to develop therapies that help improve lives and to ensure access to these therapies across ... | ||||
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Regulatory Affairs Biocides Associate Manager |
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Location: Frimley Recruiter: SC Johnson Job Hours: Full-time |
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| Registration & Regulatory Affairs BPR (Biocidal Product Registration) Associate Manager • Location: Frimley, UK • Function: GSARA (global safety assessment and regulatory affairs) About the role The Global Registration and Regulatory Compliance (GRRC) team provide regulatory leadersh... | ||||
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Global Regulatory Affairs, Associate Director (Oncology) |
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Location: Cambridge Recruiter: Gilead Sciences International |
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| Description We are looking for a driven individual who is passionate about bringing transformational medicines to those in Europe and international countries with continued unmet medical need. This is an exciting opportunity for a Regulatory Affairs Associate Director to join the Gil... | ||||
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Regulatory Affairs Associate (EU) |
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Location: Surrey Recruiter: EPM Scientific Job Hours: Full-time |
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| Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: • Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with regulatory and legal changes in EU • Preparing pre- and post-authorisation regulatory docume... | ||||
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Regulatory Affairs Associate (EU) |
Apply | |||
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Location: Surrey Recruiter: EPM Scientific Job Hours: Full-time |
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| Regulatory Affairs Associate The Regulatory Affairs Associate will be responsible for: • Managing the clinical trial applications in Europe and other selected countries • Keeping up to date with regulatory and legal changes in EU • Preparing pre- and post-authorisation regulatory docume... | ||||
