Clinical Research Associate
2 semanas atrás
At ICON, we are seeking a highly skilled Clinical Research Associate to join our team. As a Clinical Research Associate, you will play a critical role in the success of our clinical trials by ensuring the integrity of data and compliance with regulatory requirements.
Key Responsibilities:- Monitoring and Data Management: Conduct onsite and remote monitoring activities to ensure clinical trials are conducted in accordance with protocols, SOPs, and regulatory requirements.
- Site Management: Manage investigative site staff to facilitate trial deliverables, including subject enrollment and data deliverables.
- Regulatory Compliance: Verify the protection of study participants and ensure compliance with ICH-GCP guidelines and applicable regulations.
- Reporting and Escalation: Write and submit reports of investigational site findings and escalate observed deficiencies and issues as appropriate.
- Document Management: Manage essential documents as required by local regulations and ICH-GCP guidelines.
- Education: Undergraduate degree or international equivalent in a clinical, science, or health-related field from an accredited institution.
- Experience: Previous experience supporting clinical trials, including solid onsite monitoring experience.
- Location: Based in São Paulo.
- Travel: Travel required 50-80%.
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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