Senior CRA

extra holidays - extra parental leave
Work set-up: 
Full Remote
Contract: 
Experience: 
Senior (5-10 years)
Work from: 

Offer summary

Qualifications:

Advanced degree in life sciences, nursing, or medicine., Extensive experience as a Clinical Research Associate., Strong understanding of clinical trial processes and regulatory requirements., Proficiency in clinical trial software and tools..

Key responsibilities:

  • Monitoring clinical trial sites for protocol adherence and GCP standards.
  • Conducting site visits to assess performance and resolve issues.
  • Collaborating with teams to ensure accurate data collection and reporting.
  • Providing training and support to site staff and other CRAs.

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ICON plc XLarge http://www.iconplc.com
10001 Employees
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Job description

Senior CRA Remote Brazil

ICON plc is a worldleading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development

We are currently seeking a Senior Clinical Research Associate (CRA) to join our diverse and dynamic team. As a Senior CRA at ICON Plc, you will play a critical role in overseeing and managing clinical trial activities to ensure they are conducted according to protocol, regulatory requirements, and industry standards. You will contribute to the success of clinical trials by ensuring data integrity, participant safety, and compliance throughout the study lifecycle.

What You Will Be Doing:

Required profile

Experience

Level of experience: Senior (5-10 years)
Spoken language(s):
Portuguese
Check out the description to know which languages are mandatory.

Other Skills

  • Organizational Skills
  • Problem Solving
  • Social Skills
  • Communication

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