• QA, QC & Validation
• Clinical Research
• Clinical Data Management
• Medical Information
• Medical Affairs
• Regulatory Affairs
• Health Economics And Outcomes Research
• Sales & Business Development
• Marketing & Brand Management
• Scientific & Engineering
• Drug Safety & Pharmacovigilance
• Statistics & Sas

Hays Pharma provides specialised regulatory affairs talent on either a permanent or temporary basis that can be sourced on a global basis.

These professionals can be sourced as individuals or as a full project team and can assist you with a range of regulatory tasks such as clinical trial applications, regulatory submissions, liaison with regulatory authorities, importation & exportation requests, recognition filings, due diligence audits, product classification and national pricing strategy. Typical searches we undertake are for;

Regulatory Affairs Consultants - Pharma, Biotech and Medical Devices
Regulatory Affairs Executives
Directors and VP's of Regulatory.

To  search for the latest available positions, click here