Clinical Research Associate

Job Description

As a Clinical Research Associate, you will play a critical role in coordinating clinical studies and ensuring compliance with FDA regulations. This includes the preparation and oversight of protocols, participant recruitment, and monitoring trial execution to achieve successful outcomes.

Responsibilities

• Lead clinical trial inception and execution phases.
• Evaluate data quality and participant adherence.
• Provide guidance to research staff on best practices.
• Conduct detailed reviews of clinical trial reports.
• Implement improvements based on trial feedback.
• Develop and maintain strong relationships with stakeholders.
• Ensure timely communication of trial results to stakeholders.
• Collaborate to enhance protocol adherence and site performance.

Requirements

Education

• Bachelor's degree in Nursing, Pharmacy, or related field
• Advanced degree preferred

Experience

• 3+ years of experience in clinical research monitoring

Technical Skills

• Protocol Development
• Statistical Analysis
• Clinical Trial Management Software (CTMS)

Soft Skills

• Problem-solving
• Adaptability

Certifications

• Certified Clinical Research Associate (CCRA)
• ISO 14155 certification

Languages

• English: Fluent

Advantageous

• Experience in patient recruitment: History of successful patient recruitment strategies and practices.
• Familiarity with electronic data capture: Understanding of platforms utilized for electronic data capture in clinical trials.

Benefits

• Comprehensive healthcare coverage
• 401(k) plan with competitive company match
• Paid time off and holidays
• Professional development opportunities

Company Culture

• Continuous Improvement: We strive for continuous improvement, both in research practices and team development.
• Diversity and Inclusion: We are committed to diversity and creating an inclusive workplace.
• Professional Growth: Opportunities for professional growth and training are a priority for our team.