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Clinical Research Associate

2 meses atrás

São Paulo, São Paulo, Brasil Icon Tempo inteiro
About ICON

At ICON, we pride ourselves on being a leader in the clinical research industry. Our team of experts is dedicated to advancing and improving patients' lives through innovative and high-quality research.

Job Summary

We are seeking a highly motivated and experienced Clinical Research Associate to join our team. As a Clinical Research Associate, you will be responsible for managing clinical trials, ensuring compliance with regulatory requirements, and collaborating with cross-functional teams to deliver high-quality results.

Key Responsibilities
  • Manage clinical trials from initiation to close-out, ensuring compliance with regulatory requirements and ICON's SOPs/WPs.
  • Collaborate with cross-functional teams, including study teams, sites, and sponsors, to ensure timely and accurate data collection and reporting.
  • Conduct site management activities, including investigator recruitment, data entry, and query resolution.
  • Develop and maintain strong relationships with sites and investigators, ensuring a high level of satisfaction and compliance.
  • Participate in QA audits and provide support as needed.
  • Attend project-specific and departmental meetings to ensure alignment and communication.
  • Travel as needed to conduct site visits and meetings.
Requirements
  • Minimum Bachelor's degree in a life science.
  • At least 12 months of experience in a CTA/Clinical Trial Assistant or similar role within the clinical/pharmaceutical industry.
  • Understanding of ICH GCP Compliance.
  • Excellent communication and organizational skills.
  • Able to work in a fast-paced environment and prioritize multiple tasks.
What We Offer

We offer a competitive salary package, annual bonuses, and a range of health-related benefits to employees and their families. We are committed to providing a workplace free of discrimination and harassment, and we are an equal opportunity employer.