R&D, Pharmacovigilance & Regulatory Affairs_uk

  • R&D, Pharmacovilance & Regulatory Affairs

    Researching, developing, testing and launching new drug solutions. The development process lasts from 8 to 10 years and is made up of 4 phases.

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Specialist II, Pharmacovigilance, Rare Diseases (Boston, MA or Cary, NC) Cary, NC, US 25-Sep-2022 1418
R&D Supply Chain Intern
R&D Supply Chain Intern Parma, IT 25-Sep-2022 603
Parma, IT 25-Sep-2022 603
Clinical Project Manager
Clinical Project Manager Cary, NC, US 13-Sep-2022 1512
Cary, NC, US 13-Sep-2022 1512
Target Validation & New Product Evaluation Scientist Parma, IT 11-Sep-2022 1137
R&D - QA Training & Documentation Intern.
R&D - QA Training & Documentation Intern. Parma, IT 11-Sep-2022 787
Parma, IT 11-Sep-2022 787
Clinical Trial Transparency & Documentation Specialist Paris, FR 11-Sep-2022 1182
Exploratory Chemistry Intern
Exploratory Chemistry Intern Parma, IT 10-Sep-2022 1443
Parma, IT 10-Sep-2022 1443
In Vivo Pharmacology Lab Technician - Intern Parma, IT 10-Sep-2022 1097
Project Management R&D Rare Diseases - Intern Parma, IT 10-Sep-2022 712
Regulatory Operations and Compliance Manager
Regulatory Operations and Compliance Manager Cary, NC, US 10-Sep-2022 1436
Cary, NC, US 10-Sep-2022 1436
Regulatory Affairs Manager Rare Diseases - MENA Region Parma, IT 09-Sep-2022 1320
Head of Late Phase Study Management-US & Canada, Global Clinical Operations Cary, NC, US 03-Sep-2022 1313
Clinical Statistical Programmer
Clinical Statistical Programmer Parma, IT 02-Sep-2022 1413
Parma, IT 02-Sep-2022 1413
Senior Formulation Scientist
Senior Formulation Scientist Chippenham, GB 31-Aug-2022 1427
Chippenham, GB 31-Aug-2022 1427
eTMF & Data Archiving Manager
eTMF & Data Archiving Manager Parma, IT 31-Aug-2022 1488
Parma, IT 31-Aug-2022 1488