Messina is looking for an International Regulatory Affairs Subject Matter Expert to provide support of International Regulatory Affairs projects including international clinical trials and product registration and/or approval. This is expected to be an 8 to 12-month engagement. 

Regulatory affairs background, specifically has worked on:

  • Filing INDs
  • Amendments
  • Annual reports on NDAs
  • Must have expertise with international regulations ( i.e. MHRA (UK), TGA (Australia), HEALTH CANADA (CANADA), ANVISA (Brazil), EMEA (European Union), MHLW (Japan), SWISSMEDIC (Switzerland), KFDA (Korea), etc.)
  • Regulatory Affairs Experience:
    • Compiling/supporting & filing INDs
    • Compiling / supporting & filing amendments
    • Compiling/supporting & filing annual reports
    • Compiling/supporting & filing NDAs
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International Regulatory Affairs SME/Expert | Contract

Remote, IL

Messina is looking for an International Regulatory Affairs Subject Matter Expert to provide support of International Regulatory Affairs projects including international clinical trials and product registration and/or approval. This is expected to be an 8 to 12-month engagement. 

Regulatory affairs background, specifically has worked on:

  • Filing INDs
  • Amendments
  • Annual reports on NDAs
  • Must have expertise with international regulations ( i.e. MHRA (UK), TGA (Australia), HEALTH CANADA (CANADA), ANVISA (Brazil), EMEA (European Union), MHLW (Japan), SWISSMEDIC (Switzerland), KFDA (Korea), etc.)
  • Regulatory Affairs Experience:
    • Compiling/supporting & filing INDs
    • Compiling / supporting & filing amendments
    • Compiling/supporting & filing annual reports
    • Compiling/supporting & filing NDAs

Learn More:

Sarah Benz

Vice President of Talent Acquisition

sbenz@messinagroupinc.com

847.692.0618

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