Clinical Safety Specialist II

Há 3 dias


São Paulo, São Paulo, Brasil SAO Fortrea Brazil Limitada Tempo inteiro
Job Summary

As a leading global contract research organization, SAO Fortrea Brazil Limitada provides pharmaceutical, biotechnology, and medical device customers with a wide range of clinical development, patient access, and technology solutions across multiple therapeutic areas.

Key Responsibilities
  • Assist with overall Clinical Safety and/or PSS operations associated with products, including the entire adverse events process.
  • Manage and process expendable adverse events to the required standard and submit them to clients and regulatory agencies within agreed timelines.
  • Provide high-quality service to clients in a safe and cost-effective manner, ensuring compliance with legal requirements and company policies.
Requirements
  • Degree in Biological Sciences, Pharmacy, Nursing, Medical Sciences, Life Sciences, or related area.
  • Previous experience with general pharmacovigilance activities, including case processing, regulatory submissions, and quality control.
  • Fluent English and intermediate Spanish language skills.
  • General MS Office knowledge and familiarity with Good Clinical Practice (GCP) and ICH Guidelines.
  • Ability to interact with line and middle management, staff, and external contacts on a functional and tactical level.
About SAO Fortrea Brazil Limitada

We are a global contract research organization with a passion for scientific rigor and decades of clinical development experience. Our commitment is to revolutionize the development process, ensuring the swift delivery of life-changing ideas and therapies to patients in need. We are seeking motivated problem-solvers and creative thinkers who share our passion for overcoming barriers in clinical trials.



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