CRA II

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

📋 Description

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

• 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.

• Design and analyze clinical trials, interpret complex medical data, and contribute to the development 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 knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.

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

• Ability to operate independently and collaboratively in a dynamic environment.

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

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

🏝️ Benefits

• Competitive base salary

• Performance-related incentives

• Medical, dental, and vision coverage where applicable

• Retirement and pension plans

• Life assurance and disability coverage

• Employee assistance programs and wellbeing resources

• Learning and development opportunities through structured training and career pathways