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

📋 Description

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

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

• Work in partnership with investigators and site personnel to ensure seamless study execution.

• Conduct data reviews and resolve queries to uphold high-quality clinical data.

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

• Required experience in oncology monitoring.

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

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

• Capacity to work both independently and collaboratively in a fast-paced environment.

• Willingness to travel as needed, up to 60%-75% within the designated region.

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

🏝️ Benefits

• Competitive base salary along with performance-based incentives.

• Medical, dental, and vision insurance where applicable.

• Retirement and pension plans available.

• Life insurance and disability coverage.

• Employee assistance programs and wellness resources.

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