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Last profile update: 03/08/2020
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
Last profile update: 03/08/2020
11 - 20 Years experience in this/these domain(s)
Biological Scientist - Biotechnologist - Other Expert - Pharmacist - Laboratory Manager - Laboratory Project Manager - Other Expert - CMC Formulation Developper - R&D Analytical Resources - Pre-Clinical SOP Writer
Last profile update: 03/08/2020
Statistical Consultancy, Study Design and Analyses by an Independent Biostatistician
> 20 Years experience in this/these domain(s)
Statistician - Statistical Trainer
Last profile update: 02/08/2020
Quality Outsourcing Enablement
> 20 Years experience in this/these domain(s)
Clinical Project Manager - Clinical Operation Manager/ Director - Clinical Trainer - Clinical Vendor Manager - Clinical Contract Manager - Clinical Educator - Clinical Data Director - Other Expert - Contract Negociator
Last profile update: 02/08/2020
Consultant freelance for monitoring and coordinating activities of clinical trials
> 20 Years experience in this/these domain(s)
Clinical Project Manager - Clinical Research Associate - Clinical Study/Trial Manager
Last profile update: 02/08/2020
> 20 Years experience as Clinical Research Associate
> 20 Years experience in this/these domain(s)
Clinical Research Associate
Last profile update: 01/08/2020
11 - 20 Years experience in this/these domain(s)
Clinical Project Manager - Clinical Research Associate - Clinical Study/Trial Manager - Clinical Quality Assurance Manager - Clinical Contract Manager - Clinical Start-up Specialist
Last profile update: 01/08/2020
Senior Clinical Research Consultant with over 25 years experience
> 20 Years experience in this/these domain(s)
Clinical Research Associate - Lead Clinical Research Associate - Clinical Study/Trial Manager - Clinical Trainer - Clinical Quality Assurance Manager - Clinical Start-up Specialist - Clinical SOP Writer
Last profile update: 01/08/2020
Process Engineering, Technology Transfer, Validation
> 20 Years experience in this/these domain(s)
Manufacturing Engineer - Manufacturing/ Production Manager - Validation Engineer - Quality Assurance GMP specialist - Technical Services Specialist - Project Manager in GMP - Manufacturing SOP Writer
Last profile update: 01/08/2020
> 20 Years experience in this/these domain(s)
Manufacturing/ Production Manager - Quality Assurance GMP specialist - Quality Control - Quality Manager - Drug Development - Quality Validation Analyst - Drug Development Project Manager - Manufacturing SOP Writer - Quality Assurance Trainer - Quality Assurance SOP Writer - GMP Auditor - Quality Assurance Auditor - Other Auditor