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Regulatory Affairs Associate (EU)
SURREY, ENGLAND, UNITED KINGDOM
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 documentation and...
Associate Director, Clinical Pharmacology
SURREY, ENGLAND, UNITED KINGDOM
...The Associate Director, Clinical Pharmacology is responsible for leading clinical research activities with focus on clinical pharmacology phase I pharmacokinetics and bioequivalence trials. He/she will ensure that high quality expertise is provided to meet state-of-the-art scientific, industry and...
Regulatory Affairs Associate (EU)
SURREY, SOUTH EAST ENGLAND
p b Regulatory Affairs Associate /b /p p br /p p The b Regulatory Affairs Associate /b will be responsible for: /p p br /p p • Managing the clinical trial applications in Europe and other selected countries /p p • Keeping up to date with regulatory and legal changes in EU /p...
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WINDLESHAM
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Vice President Supply Chain
£100 - 125
WEYBRIDGE
...li li Experience in clinical trial labelling, supplies, logistics & distribution an advantage. br /li li Knowledge in planning, procurement and capacity a significant advantage. br /li li Exposure to Oracle ERP, Microsoft Office Suite, APICS Certification. br /li /ul br br p This...
Regulatory Affairs Associate (EU)
SURREY
...p • Managing the clinical trial applications in Europe and other selected countries /p p • Keeping up to date with regulatory and legal changes in EU /p p • Preparing pre- and post-authorisation regulatory documentation and applications /p p • Assisting in marketing...
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