Clinical Research Associate I

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

📋 Description

• Provide high-quality clinical trial monitoring services.

• Oversee all tasks related to the setup and monitoring of studies.

• Compile precise study status reports and manage study documentation.

• Address sponsor-generated queries effectively and ensure cost efficiency for the study.

• Contribute to the preparation and assessment of study documents and feasibility analyses for new proposals as needed.

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

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

⛳️ Requirements

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

• Prior experience as a Clinical Research Associate (CRA).

• Familiarity with ICH-GCP guidelines.

• Ability to review and assess medical data proficiently.

• Exceptional written and verbal communication skills in English.

• Strong interpersonal skills to handle inquiries promptly.

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

• 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 progression.