This is a fully remote position, open to applicants in Brazil.

📋 Description

• Oversee all tasks related to the initiation and monitoring of a study.

• Prepare precise study status updates and manage study documentation.

• Efficiently handle queries generated by sponsors.

• Assume responsibility for maintaining cost efficiency throughout the study.

• Contribute to the development and review of study documentation and feasibility assessments for new proposals as necessary.

• Build and sustain collaborative relationships with essential stakeholders, clinical investigators, and site personnel.

• Ensure patient safety and adherence to ICON's procedures, protocols, and regulatory standards.

⛳️ Requirements

• Bachelor's degree in medicine, science, or a related field.

• Relevant experience in clinical trial monitoring.

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data effectively.

• Strong written and verbal communication skills in English.

• Good interpersonal skills to address inquiries promptly.

• Willingness to travel as necessary (approximately 60%).

• Legal authorization to work in Brazil.

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Health and wellness programs, including medical, dental, and vision coverage where applicable.

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

• Opportunities for learning and career development through structured training and career pathways.