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

📋 Description

• Carrying out site qualification, initiation, monitoring, and close-out visits for clinical trials

• Ensuring adherence to protocols, data integrity, and patient safety throughout the trial process

• Collaborating with investigators and site personnel to ensure seamless study execution

• Conducting data reviews and resolving queries to uphold high-quality clinical data

• Assisting in the preparation and evaluation of study documents, such as protocols and clinical study reports

⛳️ Requirements

• Bachelor’s degree in a scientific or healthcare-related discipline

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

• Extensive knowledge of clinical trial processes, regulations, and ICH-GCP guidelines

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

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

• Openness to travel as needed (approximately 60%)

🏝️ Benefits

• Competitive base salary along with performance-based incentives

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

• Retirement and pension schemes

• Life insurance and disability coverage

• Employee assistance programs and wellness resources

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