Clinical Research Associate I

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

📋 Description

• Oversee all aspects of establishing and monitoring a study

• Ensure precise completion of study status reports and maintain necessary study documentation

• Efficiently manage queries generated by sponsors

• Take charge of maintaining study cost efficiency

• Engage in the preparation and evaluation of study documentation and feasibility studies for new proposals as necessary

• Cultivate and uphold collaborative relationships with key stakeholders, clinical investigators, and site personnel

• Safeguard patient safety while adhering 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 assess and interpret medical data

• Strong written and verbal communication skills in English

• Good interpersonal skills to address inquiries promptly

• Willingness to travel as needed (approximately 35%)

• Legal authorization to work in the country where the position is located

🏝️ Benefits

• Competitive base salary along with performance-based incentives

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

• Retirement and pension plans

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

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