
Clinical Research Associate II
Posted 4 days ago

Posted 4 days ago
This is a fully remote position, open to applicants in Brazil.
• Execute and document various onsite monitoring visits
• Participate in study initiation and feasibility assessments
• Conduct CRF evaluations, source document verifications, and resolve queries
• Manage site communication and oversight
• Serve as a liaison for in-house support services and vendors
• Update internal project teams on study advancements
• Assist the regulatory team in preparing necessary documents for study submissions
• Bachelor's degree in Life Sciences or a comparable combination of education, training, and experience
• Experience in independent onsite monitoring
• Familiarity with various types of monitoring visits in Phase II / III
• Background in Oncology is preferred
• Fluency in English and Spanish
• Competence in MS Office applications
• Capability to plan and collaborate effectively in a dynamic team setting
• Strong communication, collaboration, and problem-solving abilities
• Willingness to travel
• Chance to enhance skill sets
• Opportunity to expand therapeutic area knowledge
• Potential to become a specialist in clinical research
ICON plc
ICON plc
Parexel
Thermo Fisher Scientific
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