Pharmaceutical Regulatory Consultant

1 day ago


Gothenburg, Västra Götaland, Sweden Randstad - Göteborg Full time
About the Role:
We are seeking a Regulatory Information Management Specialist to join our team at Randstad Life Science. As a key member of our global team, you will be responsible for ensuring efficient and seamless Regulatory Information Management across all stages. Your expertise in areas vital to successful RIM execution will enable us to stay ahead in the dynamic world of pharmaceuticals.

Responsibilities:
  • Collaborate with teams to ensure efficient and seamless Regulatory Information Management.
  • Oversee the regulatory data for assigned areas, ensuring alignment with industry standards, regulatory requirements, and business processes.
  • Prepare and submit regulatory data submissions (XEVMPD, IDMP, etc.) to health authorities.

What We're Looking For:
  • A university degree in life sciences or equivalent experience in the pharmaceutical/medical industry.
  • A strong understanding of the pharmaceutical drug development process.
  • Excellent analytical and critical thinking abilities.


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