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  • Anonymous

    Last profile update: 01/12/2021

    Consultant vaccines technical development & registration

    > 20 Years experience in this/these domain(s)

    Biological Scientist - Biotechnologist - Molecular Biologist - Medical Advisor - Medical Director - Medical Manager - Medical Writer - CMC/ Regulatory Manager - Other Expert - Regulatory Affairs Director - Regulatory Affairs Manager - Regulatory Affairs Officer - Medical Writer - Other Expert - Drug Development - Quality Process Analyst - Quality Validation Analyst - Drug Development Project Manager - R&D Analytical Resources - Regulatory Affairs Trainer

    • Andorra
    • from 91 / Hour
      • 20% Dec
      • 40% Jan
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    updated
  • Anonymous

    • Certified

    Last profile update: 01/12/2021

    11 - 20 Years experience in this/these domain(s)

    Clinical Project Manager - Lead Clinical Research Associate - Clinical Study/Trial Manager - Clinical Vendor Manager - Clinical Contract Manager - Clinical Start-up Specialist - TMF Management

    • United Kingdom
      Antrim
    • from 71 /Hour
      • 60% Dec
      • 100% Jan
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    new
  • Anonymous

    Last profile update: 24/11/2021

    Data Manager with 13+ years experience and sound knowledge on Onco studies. Worked on RAVE, OC, SAS-Pheedit Etc

    11 - 20 Years experience in this/these domain(s)

    Clinical Project Manager - Clinical Study/Trial Manager - Clinical Trainer - Clinical Start-up Specialist - Clinical Data Director - Clinical Data Manager - Clinical Data Associate - Clinical Data Entry Manager - Data Management Application Manager - Data Integration Specialist - Data Extraction and Transformation Specialist - Clinical Data Report Generation Specialist - Data Management Trainer

    • India
      Andhra Pradesh
    • from 51 /Hour
      • 40% Dec
      • 40% Jan
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  • Anonymous

    • Certified

    Last profile update: 22/11/2021

    11 - 20 Years experience in this/these domain(s)

    Quality Assurance GMP specialist - Project Manager in GMP - Scientific Translator - Quality Manager - Quality Process Analyst - Manufacturing SOP Writer - Quality Assurance Trainer - Quality Assurance SOP Writer - GMP Auditor - Quality Assurance Auditor

    • Belgium
      Brussels
    • Not disclosed
      • 100% Dec
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  • Anonymous

    • Certified

    Last profile update: 17/11/2021

    1 - 3 Years experience in this/these domain(s)

    CMC Formulation Developper

    • India
      Maharashtra
    • < 50 / Hour
      • 100% Dec
      • 100% Jan
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  • Anonymous

    Last profile update: 15/11/2021

    Clinical Trial Educator

    4 - 10 Years experience in this/these domain(s)

    Biological Scientist - Biotechnologist - Molecular Biologist - Other Expert - Medical Writer - Other Expert - Clinical Project Manager - Clinical Research Associate - Clinical Study/Trial Manager - Clinical Trainer - Clinical Educator - Other Expert - Other Expert - Other Expert - Other Expert - Other Expert - Market Researcher - Public Relations Specialist - Other Expert - Other Expert - Quality Assurance GLP Specialist - Laboratory Manager - Laboratory Project Manager - Other Expert - Other expert - Open Innovation - Contract Negociator - Trainer - Medical Affairs Trainer - Pre-Clinical SOP Writer - Pre-Clinical Trainer

    • Argentina
      Argentine Northwest
    • < 50 / Hour
      • 20% Dec
      • 20% Jan
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      • 20% May
  • Anonymous

    • Certified

    Last profile update: 13/11/2021

    1 - 3 Years experience in this/these domain(s)

    Bioinformatician - Genetics and Genomics Scientist - Molecular Biologist

    • Turkey
      Marmara Region
    • < 50 / Hour
      • 80% Dec
      • 60% Jan
      • 80% Feb
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  • Anonymous

    • Certified

    Last profile update: 09/11/2021

    11 - 20 Years experience in this/these domain(s)

    Qualified Person - Quality Assurance Trainer - GMP Auditor - Quality Assurance Auditor

    • India
      Delhi
    • < 50 / Hour
      • 80% Dec
      • 80% Jan
      • 80% Feb
      • 80% Mar
      • 80% Apr
      • 80% May
  • Anonymous

    Last profile update: 02/11/2021

    11 - 20 Years experience in this/these domain(s)

    Clinical Research Associate - Clinical Start-up Specialist

    • Turkey
      Marmara Region
    • from 71 /Hour
      • 40% Dec
      • 50% Jan
      • 50% Feb
      • 50% Mar
      • 50% Apr
      • 50% May
  • Anonymous

    Last profile update: 01/11/2021

    Regulatory Affairs Specialist

    11 - 20 Years experience in this/these domain(s)

    Clinical Research Associate - Manufacturing/ Production Manager - Packaging and Labelling Specialist - Purchasing/ Procurement Specialist - Quality Assurance GMP specialist - Project Manager in GMP - CMC/ Regulatory Manager - Regulatory Affairs Manager - Regulatory Affairs Officer - Regulatory Affairs Administrator - Medical Writer - Regulatory Submission Manager - Pharmacist - Pharmaceutical Pharmacist - Scientific Translator - Qualified Person - Manufacturing SOP Writer

    • Albania
    • < 50 / Hour
      • 0% Dec
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