68 Drug Development Jobs in Stevenage
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Statistics Leader / Associate Director of Statistics GlaxoSmithKline - Stevenage, England, United Kingdom Our end-to-end project support model ensures that our statisticians have the opportunity to work across the entire range of drug development, from early clinical development to registration and marketed... 2 days ago
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Director, Clinical Research and Early Programmes Immunology Stevenage, England, United Kingdom And/or accountability for design and delivery of the full development clinical development plan that effectively demonstrates benefit-risk and leads to a successful submission to regulators, payors etc... 16 days ago
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Clinical Development Director - Hepatology GlaxoSmithKline - Stevenage SG1, UK Experience in clinical drug development with an understanding of the hepatology disease space, the underlying biology, and potential therapeutic targets, as well as current and future potential treatment... More than 30 days ago
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Associate Director/Director, Quantitative Systems Pharmacology GlaxoSmithKline - Stevenage SG1, UK Work in close collaboration with biologists, clinicians, clinical pharmacologists, pharmacometricians, statisticians and other partner line colleagues to inform research and development programs and improve... More than 30 days ago
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JUNIOR MEDICINAL CHEMIST Autifony Therapeutics - Stevenage, England Autifony is a cutting-edge biotech company dedicated to developing new medicines to treat rare genetic CNS disorders by deploying its pioneering ion channel drug discovery platform. Since its formation... £31K - £44K (Glassdoor Est.) 15 days ago
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RWD Manager | Regulatory Affairs | Early Access Program SEC Life Sciences - Hitchin SG5, Hertfordshire, Eastern Lead and manage projects involving Real World Evidence (RWE), integrating these insights with Regulatory Affairs to optimise early access programmes. Design and implement strategies to gather and utilise... Yesterday
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Bioanalytical Scientists Pharmidex - Hatfield, United Kingdom · Ideally you will have at least two years of experience of working in a bioanalytical laboratory where you were responsible for LC-MS method development and validation. · A good working knowledge of sample... Today
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LC-MS Research Scientist - Proteomics VRS-UK - Cambridge, Cambridgeshire, United Kingdom You will be responsible for developing & optimizing these LC-MS biomarker methods, analysing complex data sets and contributing towards the continuous improvement of existing assays and taking a leading... £32000 - £45000/annum 4 days ago
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Senior Trial Master File Study Owner Pharmalex - Tring, Hertfordshire, United Kingdom, United Kingdom The Senior Trial Master File Study Owner provides pivotal support and subject matter expertise (SME) at a study level, proactively ensuring our clients’ Trial Master Files (TMFs) are achieving an inspection... 11 days ago
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Regulatory Manager, Devices Ware, England, United Kingdom When applying for this role, please use the ‘cover letter’ of the online application or your CV to describe how you meet the competencies for this role, as outlined in the job requirements above. The information... 14 days ago
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