Clinical Research Associate I

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

📋 Description

• Managing and coordinating clinical trials, ensuring adherence to regulations, and gathering as well as analyzing vital data.

• Overseeing all tasks related to the establishment and monitoring of a study, preparing precise study status reports, and maintaining documentation related to the study.

• Efficiently handling sponsor-generated inquiries and taking charge of the cost-effectiveness of the study.

• Engaging in the preparation and evaluation of study documentation and feasibility assessments for new proposals as necessary.

• Building and sustaining strong, collaborative relationships with key stakeholders, clinical investigators, and site personnel.

• Safeguarding patient safety by ensuring compliance with ICON’s procedures, protocols, and regulatory standards.

⛳️ Requirements

• A university degree in medicine, science, or a related field.

• Familiarity with ICH-GCP guidelines and the ability to review and assess medical data.

• Exceptional written and verbal communication skills in English (mandatory).

• Strong interpersonal skills that enable timely responses to inquiries.

• Willingness to travel at least 60% of the time (both internationally and domestically - by air and road) and must hold a valid driver's license.

🏝️ Benefits

• Various annual leave entitlements.

• A variety of health insurance options to meet the needs of you and your family.

• Competitive retirement planning solutions that help maximize savings and allow for confident future planning.

• Global Employee Assistance Programme, TELUS Health, providing 24-hour access to a worldwide network of over 80,000 independent specialized professionals dedicated to supporting your and your family’s well-being.

• Life assurance.

• Flexible country-specific optional benefits, which may include childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments, and more.