Clinical Trial Professional

Há 2 dias


São Paulo, São Paulo, Brasil beBeeResearch Tempo inteiro US$120.000 - US$140.000
Clinical Research Associate

We are currently seeking a dedicated and detail-oriented Clinical Research Associate to join our dynamic team. As a key member of our research department, you will be responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

Key Responsibilities:
  • Coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation.
  • Efficiently run sponsor generated queries and take responsibility for study cost efficiency; participate in the preparation and review of study documentation and feasibility studies for new proposals as required.
  • Develop and maintain strong, collaborative relationships with key stakeholders, clinical investigators, and site staff.
  • Ensure patient safety by ensuring compliance with procedures, protocols, and regulatory requirements.
Requirements:
  • Minimum of 2 years of experience as a CTA, Study Coordinator, IHCRA.
  • Deep understanding of ICH GCP Compliance.
  • Excellent English - writing, reading, communication.
  • Highly motivated with a phenomenal eye for detail.
  • Complete Bachelor's degree in life science or related discipline.
  • Ability to travel at least 60% of the time (international and domestic) and possess a valid driver's license.


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