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

📋 Description

• Perform site qualification, initiation, monitoring, and closure visits for clinical trials.

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

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

• Conduct data reviews and resolve inquiries to uphold the quality of clinical data.

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

• Operate within a sponsor-dedicated framework, benefiting from ICON’s extensive global expertise.

• Assume accountability for deliverables while fostering collaborative work relationships.

⛳️ 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 skills, with a keen attention to detail.

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

• Residing in California or Colorado in proximity to a major airport.

• Open to travel as necessary, up to 60-75% within the designated region.

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

🏝️ Benefits

• Competitive base salary.

• Incentives based on performance.

• Comprehensive medical coverage.

• Dental coverage.

• Vision coverage.

• 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.