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

📋 Description

• Conduct site evaluations, initial assessments, monitoring, and closing visits for clinical trials.

• Ensure adherence to protocols, maintain data integrity, and prioritize patient safety throughout the trial stages.

• Work in partnership with investigators and site personnel to promote efficient study execution.

• Review data and resolve inquiries to uphold high standards of clinical data quality.

• Assist in the drafting and examination of study documentation, such as protocols and clinical study reports.

• Design and evaluate clinical trials, interpret intricate medical data, and contribute to the development of innovative treatments and therapies.

⛳️ Requirements

• A Bachelor's degree in a scientific or healthcare-related discipline.

• At least 2 years of experience as a Clinical Research Associate.

• Comprehensive understanding of clinical trial procedures, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication skills, with a keen eye for detail.

• Capability to work both independently and as part of a team in a dynamic environment.

• Readiness to travel as needed (approximately 60%).

• Legal authorization to work in Chile.

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension schemes.

• Life insurance and disability coverage.

• Employee assistance programs and wellbeing resources.

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