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

📋 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.

• Work in collaboration with investigators and site personnel to facilitate effective study execution.

• Execute data review and address queries to uphold high standards of clinical data quality.

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

• Assume responsibility for clinical trial monitoring deliverables and engage collaboratively in a sponsor-dedicated model.

⛳️ Requirements

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

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

• Experience in oncology monitoring is essential.

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

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

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

• Willingness to travel as necessary, approximately 60%-75% within the region (Western preferred, but open to any location).

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

🏝️ Benefits

• Competitive base salary along with performance-related incentives.

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

• Retirement and pension plans.

• Life insurance and disability coverage.

• Employee assistance programs and resources for wellbeing.

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