Regulatory Affairs Specialist

il y a 3 jours


Paris, Île-de-France Apsida Life Science Temps plein
Global Regulatory Affairs Consultant

Apsida Life Science has partnered with a leading Pharmaceutical company to seek a Global Regulatory Affairs Consultant.

The Global Regulatory Affairs Consultant will lead global regulatory strategies for marketing authorization submissions across emerging markets.

Key Responsibilities:

  • Coordinate teams to update core documentation and generate country-specific data for submissions.
  • Work closely with local teams and report key issues to senior management.

Requirements:

  • Strong regulatory expertise and knowledge of global regulatory affairs.
  • Excellent communication and collaboration skills.

About Apsida Life Science:

Apsida Life Science is a leading provider of life science solutions. We partner with pharmaceutical companies to deliver innovative solutions that meet their regulatory needs.


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