Clinical Research Associate

Job Description

Join our esteemed team as a Clinical Research Associate (CRA). In this pivotal role, you will oversee clinical trials, ensuring compliance with regulatory requirements while contributing to essential patient research. Your expertise will help drive advancements in medical treatment and enhance patient safety.

Responsibilities

• Conduct regular training sessions for site staff on the clinical trial protocols.
• Assist in the preparation and submission of IRB applications and reports.
• Ensure accurate and timely documentation of site activities in study records.
• Actively participate in quality assurance activities to uphold data integrity.
• Support budget monitoring and financial assessments related to study sites.
• Foster strong relationships with site personnel to facilitate smooth project execution.

Requirements

Education

• Relevant certification or degree

Experience

• 3+ years in clinical research or clinical trial management

Technical Skills

• Project Management
• Clinical Data Management Systems

Soft Skills

• Problem-Solving
• Leadership

Certifications

• Certified Clinical Research Associate (CCRA)

Languages

• English: Fluent

Advantageous

• Familiarity with Electronic Data Capture (EDC) systems: Experience using EDC systems for data collection and management.
• Knowledge of Good Manufacturing Practices (GMP): Understanding of GMP regulations that govern research in clinical contexts.

Benefits

• Health, dental, and vision insurance
• Support for continuing education and certification
• Work-life balance initiatives
• Annual company retreats

Company Culture

• Innovation-Driven: We encourage creative thinking and innovative problem-solving in our research processes.
• Focus on Growth: Our company supports personal and professional growth through continuous training and mentorship.