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Regulatory Affairs Specialist

2 meses atrás

São Paulo, São Paulo, Brasil Parexel Tempo inteiro

Key Responsibilities:

As a Regulatory Affairs Consultant at Parexel, you will be responsible for managing and coordinating the regulatory submission strategy for a large number of clinical trials in Brazil. This will involve:

  • Coordinating and managing the flow of information related to regulatory submissions
  • Tracking project progress and identifying potential issues
  • Collaborating with cross-functional teams to ensure regulatory compliance
  • Developing and implementing strategies to improve regulatory submission efficiency

Requirements:

To be successful in this role, you will need:

  • Strong knowledge of regulatory affairs and clinical trials
  • Excellent communication and leadership skills
  • Ability to work in a team-oriented environment
  • Detail-oriented and flexible

What We Offer:

Parexel is a leading provider of clinical research services, and we offer a dynamic and challenging work environment. As a Regulatory Affairs Consultant, you will have the opportunity to work on high-profile projects and contribute to the success of our clients.