You are looking for a freelancer working in life sciences sector such as in pharma, biotechnology, devices, CRO, nutrition, veterinary or cosmetic? You found the right place. Cortexpert is the fastest provider to find qualified freelancers to fulfill your company's needs. Cortexpert has an online freelancer database that you may consult to see available freelancers. Cortexpert is also by your side to select the freelancer you are looking for and set-up contract as per your preference. Just tell us your requirements and get your freelancers now!
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
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
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
Last profile update: 27/09/2021
Sr. freelance Clinical Research Associate
> 20 Years experience in this/these domain(s)
Clinical Research Associate
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
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
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
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
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
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