Clinical Research Associate

Há 2 horas


São Paulo, São Paulo, Brasil ICON Tempo inteiro
Job Summary

We are seeking a highly skilled Clinical Research Associate to join our team at ICON. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring patient safety and data integrity.

Key Responsibilities
  • Conduct onsite and remote monitoring activities to ensure clinical trials are conducted in accordance with ICH-GCP guidelines, applicable regulations, and SOPs.
  • Verify the protection of study participants by confirming informed consent procedures and protocol adherence.
  • Ensure the integrity of clinical data and compliance with approved protocol, GCP, and applicable regulations.
  • Manage investigative site staff to facilitate trial deliverables, including subject enrollment and data deliverables.
  • Verify proper management and accountability of Investigational Product (IP).
  • Write and submit reports of investigational site findings and updates to tracking systems.
  • Manage essential documents as required by local regulations and ICH-GCP guidelines.
  • Perform key risk assessment and management responsibilities throughout the project.
  • Participate in audit preparation and follow-up activities as needed.
Requirements
  • Undergraduate degree or international equivalent in a clinical, science, or health-related field from an accredited institution.
  • Previous experience supporting clinical trials, including solid onsite monitoring experience.
  • Based in São Paulo.
  • Travel required 50-80%.
What We Offer

At ICON, we offer a comprehensive and competitive total reward package that comprises base pay, variable pay, and recognition programs. Our best-in-class employee benefits, supportive policies, and wellbeing initiatives are tailored to support you and your family at all stages of your career.

We are an equal opportunity and inclusive employer, committed to providing a workplace free of discrimination and harassment. All qualified applicants will receive equal consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, or protected veteran status.


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