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Job TitleROW Regulatory Intelligence Data Manager - 12 Months - CambridgeA project to develop an in-house ROW regulatory intelligence database is curr
Description: Summary (Main purpose of the job) This position is responsible for supporting the activities of the Design Owning Organization at the co
Description: Ideally to start ASAP Investigating and complaints Batch review Key candidate must haves: Excellent written and verbal communicatio
Global pharmaceutical company seeking experienced technical writer to join their busy team on a contract basis.
Description: Provide information insight and data analysis, drive execution of transactional/tactical tasks to ensure Amgen Contract Manufacturing (AC
Clinical data reviewer / clinical research nurse who can technically review data from Oncology trials - work remotely in UK - hourly rate of pay
Description: The Specialist QA is a position within the Quality Regional Work Cell in Europe reporting to the Senior Manager, QA (ESQ). The QA Specia
Andy Leake at CK Clinical is recruiting for a Clinical Project Manager join a small, oncology specialised pharmaceutical company on a 6-month contr...
Andy Leake at CK Clinical is recruiting for an Epidemiologist to join a world leading innovative pharmaceutical company on a contract basis. This ...
An excellent opportunity has arisen to join a leading pharmaceutical company as a Clinical Research System Implementation Leader. The Systems Imple...
Hobson Prior is currently recruiting for a Clinical Trial Management Associate position based in Uxbridge on a 12-month contract basis. This is an ...
Quality Assurance Specialist required for a global pharmaceutical company to ensure that manufacturing processes in compliance with GMP.
Exciting work opportunity with a leading pharmaceutical company's Genomics Research area, you will be working as part of a dynamic team in a cutting e
France 6-month Freelance SCRA contract: can be home based from the Paris area or following towns: Nantes, Lille, Lyon, Bordeaux or Toulouse