Clinical Trial Manager

Há 3 dias


São Paulo, São Paulo, Brasil Medpace, Inc. Tempo inteiro
Regulatory Submissions Manager Job Summary

Medpace, Inc. is seeking a full-time Regulatory Submissions Manager to join our Study Start Up team in Sao Paulo. This role plays a key part in the clinical trial management process, utilizing expertise to develop and grow a career in a dynamic environment.

Key Responsibilities:
  • Efficiently manage and successfully execute clinical trial submissions.
  • Collaborate with cross-functional teams to ensure timely and accurate submissions.
  • Develop and maintain regulatory knowledge to stay up-to-date with industry requirements.
What You'll Bring:
  • Proven experience in clinical trial management or regulatory affairs.
  • Strong understanding of regulatory submissions and clinical trial operations.
  • Excellent communication and project management skills.

At Medpace, we offer a dynamic work environment, opportunities for growth and development, and a commitment to excellence in clinical research.



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