Clinical Research Associate

This is a fully remote position, open to applicants in California, +3 more states.

📋 Description

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

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

• Collaborate with investigators and site personnel to ensure seamless study execution.

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

• Assist in the preparation and assessment of study documentation, including protocols and clinical study reports.

• Take ownership of clinical trial monitoring deliverables and work collaboratively with the team.

• Travel as needed, approximately 60% of the time.

⛳️ Requirements

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

• A minimum of 2 years of experience as a Clinical Research Associate.

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

• Experience in monitoring Ophthalmology trials or across multiple therapeutic areas.

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

• Capability to work both independently and as part of a team in a fast-paced environment.

• Willingness to travel as required, approximately 60% of the time.

• Legal authorization to work in the country where the position is located.

🏝️ Benefits

• Competitive base salary.

• Performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

• Learning and development opportunities through structured training and career pathways.

• Reasonable accommodations provided during the recruitment process.

• An inclusive and accessible workplace.