Clinical Research Associate

Job Description

As a Clinical Research Associate, you will be integral in coordinating clinical trials, collecting and analyzing data, and supporting study compliance efforts at our San Diego facility.

Responsibilities

• Coordinate all aspects of clinical trials including planning, execution, and closeout.
• Monitor clinical site activities to ensure compliance and quality standards.
• Assist in the preparation of study protocols and associated documentation.
• Review and verify data for accuracy and compliance with study protocols.
• Provide support in audits and inspections by regulatory agencies.
• Collaborate with clinical teams to develop strategies for trial management.
• Prepare and maintain project documentation in accordance with regulatory requirements.

Requirements

Education

• Bachelor's degree in Clinical Research or related field
• Master's degree preferred

Experience

• 3+ years of experience in clinical trial monitoring or related field

Technical Skills

• Data Analysis
• Protocol Development

Soft Skills

• Problem Solving
• Teamwork

Certifications

• Certified Clinical Research Associate (CCRA)
• Good Clinical Practice (GCP) Certification

Languages

• English: Fluent

Advantageous

• Experience with Remote Monitoring Techniques: Knowledge of remote monitoring procedures for clinical trials.
• Familiarity with Patient Recruitment Strategies: Experience in developing and implementing patient recruitment strategies.

Benefits

• Comprehensive health, dental, and vision insurance
• 401(k) plan with company match
• Generous paid time off policy
• Employee wellness programs

Company Culture

• Personal Development: We are committed to the continuous development of our staff, providing ample training opportunities.
• Diversity and Inclusion: We embrace diversity and ensure that each team member’s voice is heard and respected.
• Work-Life Balance: We believe in maintaining a healthy work-life balance, offering flexible scheduling options.