Clinical Research Associate II

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

📋 Description

• Participate in monitoring activities for clinical trials, taking ownership of your responsibilities and collaborating effectively.

• Execute 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.

• Work together with investigators and site personnel to ensure the smooth execution of studies.

• Conduct data reviews and address queries to uphold the quality of clinical data.

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

⛳️ Requirements

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

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

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

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

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life assurance and disability coverage.

• Employee assistance programs and wellness resources.

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