CRA II

This is a fully remote position, open to applicants in California, +1 more state.

📋 Description

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

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

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

• Conduct data review and resolve queries to uphold high standards of clinical data quality.

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

• Design and analyze clinical trials, interpret complex medical data, and help in the advancement of innovative treatments and therapies.

⛳️ Requirements

• 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 processes, regulations, and ICH-GCP guidelines.

• Excellent organizational and communication abilities, with a keen attention to detail.

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

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

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

• Medical, dental, and vision insurance where applicable.

• Retirement and pension plans available.

• Life insurance and disability coverage provided.

• Employee assistance programs and wellbeing resources offered.

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