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  • Anonymous

    • Certified

    Last profile update: 15/10/2021

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

    Toxicologist - Drug Safety Officer/Associate - Medical Writer - Clinical Project Manager - Clinical Operation Manager/ Director - Clinical Research Associate - Lead Clinical Research Associate - Clinical Research Investigator - Clinical Site Research Co-ordinator - Clinical Study/Trial Manager - Clinical Trainer - Clinical Supplies Specialist - Clinical Quality Assurance Manager - Clinical Trial Assistant - Clinical Contract Manager - Clinical Start-up Specialist - Clinical Educator - Regulatory Affairs Director - Regulatory Affairs Manager - Regulatory Affairs Officer - Regulatory Affairs Administrator - Medical Writer - Regulatory Submission Manager - Scientific Translator - Pharmacovigilance and drug database administrator - Advisory consultant on software - Drug Development - Drug Development Project Manager - Trainer - Clinical SOP Writer - Pharmacovigilance SOP Writer - Medical Affairs Trainer - Pharmacovigilance Trainer - Pre-Clinical Trainer - Quality Assurance Trainer - Quality Assurance SOP Writer - GCP Auditor - Quality Assurance Auditor - Regulatory Affairs Trainer - TMF Management

    • India
      Karnataka
    • Not disclosed
      • 100% Oct
      • 100% Nov
      • 100% Dec
      • 100% Jan
      • 100% Feb
      • 100% Mar
    updated
  • Anonymous

    Last profile update: 14/10/2021

    13+ years of experience in pharmaceutical/biotechnology industry in QA/QC

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

    Regulatory Affairs Officer - Laboratory Technician - Quality Assurance GLP Specialist - Laboratory Manager - Other Expert - Quality Control - Quality Manager - Other Expert - R&D Analytical Resources - Quality Assurance Trainer - Quality Assurance SOP Writer - GMP Auditor - GLP Auditor - Quality Assurance Auditor - Other Auditor - Regulatory Affairs SOP Writer - Regulatory Affairs Trainer

    • India
      Andhra Pradesh
    • < 400 / Day
      • 100% Oct
      • 100% Nov
      • 100% Dec
      • 100% Jan
      • 100% Feb
      • 100% Mar
    new
  • Anonymous

    Last profile update: 12/10/2021

    Clinical Trial Liaison, MD, Europe

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

    Clinical Research Associate - Lead Clinical Research Associate - Clinical Study/Trial Manager - Clinical Start-up Specialist - Other Expert

    • Poland
      Southern Poland
    • from 81 / Hour
      • 0% Oct
      • 0% Nov
      • 0% Dec
      • 0% Jan
      • 0% Feb
      • 0% Mar
    updated
  • Anonymous

    • Certified

    Last profile update: 27/09/2021

    Sr. freelance Clinical Research Associate

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

    Clinical Research Associate

    • Belgium
      Flemish Brabant
    • from 91 / Hour
      • 0% Oct
      • 0% Nov
      • 0% Dec
      • 80% Jan
      • 80% Feb
      • 80% Mar
  • Anonymous

    Last profile update: 23/09/2021

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

    Biological Scientist - Biotechnologist - Other Expert - Medical Writer - Medical Writer - Pharmacist - Laboratory Manager - Laboratory Project Manager - Other Expert - CMC Formulation Developper - R&D Analytical Resources - Pre-Clinical SOP Writer

    • France
      Alsace
    • from 801 / Day
      • 60% Oct
      • 60% Nov
      • 60% Dec
      • 100% Jan
      • 100% Feb
      • 100% Mar
  • Anonymous

    • Certified

    Last profile update: 20/09/2021

    Clinical Research Consultant

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

    Clinical Project Manager - Clinical Operation Manager/ Director - Packaging and Labelling Specialist - Project Manager in GMP

    • Belgium
      Liège
    • Not disclosed
      • 0% Oct
      • 80% Nov
      • 80% Dec
      • 80% Jan
      • 80% Feb
      • 80% Mar
  • Anonymous

    Last profile update: 17/09/2021

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

    Clinical Project Manager - Clinical Operation Manager/ Director - Clinical Research Associate - Lead Clinical Research Associate - Clinical Site Research Co-ordinator - Clinical Study/Trial Manager - Clinical Trainer - Clinical Vendor Manager - Clinical Contract Manager - Clinical Start-up Specialist - Other Expert

    • Belgium
    • Not disclosed
      • 0% Oct
      • 0% Nov
      • 0% Dec
      • 0% Jan
      • 0% Feb
      • 0% Mar
  • Anonymous

    Last profile update: 09/09/2021

    Experienced Regulatory Affairs professional

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

    CMC/ Regulatory Manager - Regulatory Submission Manager - Regulatory Operations (publishing) - Regulatory Affairs SOP Writer

    • India
      Uttar Pradesh
    • < 50 / Hour
      • 100% Oct
      • 100% Nov
      • 100% Dec
      • 100% Jan
      • 100% Feb
      • 100% Mar
  • Anonymous

    Last profile update: 09/09/2021

    Solutions for all kinds of Pharmaceutical Industry issues

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

    Manufacturing Engineer - Manufacturing/ Production Manager - Packaging and Labelling Specialist - Validation Engineer - Quality Assurance GMP specialist - Technical Services Specialist - Project Manager in GMP - CMC/ Regulatory Manager - Other Expert - Regulatory Affairs Manager - Quality Assurance GLP Specialist - Laboratory Manager - Quality Control - Quality Manager - Other Expert - Drug Development - CMC Formulation Developper - Quality Process Analyst - Quality Validation Analyst - Drug Development Project Manager - R&D Analytical Resources - Manufacturing SOP Writer - Quality Assurance Trainer - Quality Assurance SOP Writer - GMP Auditor - GLP Auditor - Quality Assurance Auditor - Other Auditor - Regulatory Affairs SOP Writer

    • India
      Andhra Pradesh
    • Not disclosed
      • 80% Oct
      • 80% Nov
      • 80% Dec
      • 80% Jan
      • 80% Feb
      • 80% Mar
  • Anonymous

    Last profile update: 26/08/2021

    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

    • United Kingdom
      Kent
    • from 91 / Hour
      • 0% Oct
      • 0% Nov
      • 0% Dec
      • 20% Jan
      • 20% Feb
      • 20% Mar