How do they match: Regulatory Affairs Specialists

  • Drug Regulatory Affairs Specialist
  • Clinical Quality Assurance Associate
  • Clinical Quality Assurance Specialist
  • Risk and Compliance Analyst

  • Advise project teams on subjects such as premarket regulatory requirements, export and labeling requirements, or clinical study compliance issues.
  • Review clinical protocols to ensure collection of data needed for regulatory submissions.
  • Review adverse drug reactions and file all related reports in accordance with regulatory agency guidelines.

  • Advise others on legal or regulatory compliance matters.