Job Board

Regulatory Affairs Contract Opportunities

 

Join our network: Pharmalink Consulting, the most successful specialist in Worldwide Regulatory Affairs.

In a matter of weeks, Pharmalink had helped John* take control of his career: his choice of project, excellent rates of pay, flexible working arrangements.

  • Well established Consultancy with over 12 years’ experience.
  • Easy on-line timesheet system. Dedicated Finance contact. Regular payment.
  • Projects to suit your needs: flexible working hours, on-site or remote projects.
  • Access to range of projects; major Blue-Chip corporations to small start-up companies.
  • Choose from variety of Regulatory projects; pre- and post-approval; junior to strategic roles.

 

Email today for consultation with one of our commercial team. We will be happy to tell you about the opportunities we have to suit you!

Location
Various

Client

Job Type
Contract / Interim positions



Interested? Apply Now.


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  10. Relevant Skills
  11. Prescription Drugs*
  13. Biotech*
  15. Devices*
  17. OTC*
  19. Generics*
  21. CMC eg review/preparation of QOS*
  23. Manufacturing compliance*
  25. Audit work eg CMP, GLP, GCP*
  27. Clinical eg review of protocols, IB, CSRs, Module 2 & 5 documents*
  29. Postmarketing maintenance eg variations/sNDA, postmarketing commitments/safety reporting*
  31. Regulatory operations eg CTD/eCTD/dossier preparation*
  33. Original NDA/MAA filings*
  35. Labeling*
  37. Advertising and promotion*
  39. Regulatory strategy eg RA meetings, filing strategy*
 


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