Clinical Research Associate I – II

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

📋 Description

• Manage all aspects of establishing and monitoring a study.

• Produce precise study status reports and maintain comprehensive study documentation.

• Efficiently handle sponsor-generated queries and ensure cost-effectiveness for the study.

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

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

• Safeguard patient safety by adhering to ICON procedures, protocols, and regulatory standards.

• Supervise and coordinate clinical trials, ensuring compliance with regulations while collecting and analyzing vital data.

⛳️ Requirements

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

• Familiarity with ICH-GCP guidelines.

• Proficiency in reviewing and assessing medical data.

• Strong written and verbal communication skills in English.

• Effective interpersonal skills for timely resolution of queries.

• Willingness to travel a minimum of 60% of the time, both internationally and domestically.

• Valid driver's license.

• Authorized to work in Brazil.

🏝️ Benefits

• Competitive base salary.

• Performance-based incentives.

• 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.