Clinical Research Associate

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

📋 Description

• Executing clinical trial monitoring tasks to a high standard

• Overseeing all processes involved in the setup and monitoring of a study

• Producing precise study status reports and managing study documentation

• Efficiently addressing sponsor-generated queries

• Contributing to the preparation and assessment of study documents and feasibility studies for new proposals as necessary

• Building and nurturing strong, collaborative relationships with essential stakeholders, clinical investigators, and site personnel

• Ensuring patient safety by adhering to ICON's procedures, protocols, and regulatory standards

⛳️ Requirements

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

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

• Experience in Clinical Research as a CTA or in comparable positions

• Exceptional written and verbal communication skills in English

• Strong interpersonal skills, allowing for timely resolution of queries

• Openness to travel as needed (approximately 60%)

🏝️ Benefits

• Competitive base salary along with performance-related 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 pathways