Clinical Research Associate III

The Opportunity:
Monitor clinical trials and ensure protocol compliance
Coordinate with investigators and study sites
Manage clinical trial documentation and reporting
Ensure adherence to regulatory and ethical guidelines
Support clinical data collection and analysis

Who You Are:
• 10 years of experience
• Strong problem-solving skills
• Excellent communication abilities
• Knowledge of industry best practices

Preferred (Optional):
Certification in clinical research preferred

Nesco Resource offers a comprehensive benefits package for our associates, which includes a MEC (Minimum Essential Coverage) plan that encompasses Medical, Vision, Dental, 401K, and EAP (Employee Assistance Program) services.

Nesco Resource provides equal employment opportunities to all employees and applicants for employment and prohibits discrimination and harassment of any type without regard to race, color, religion, age, sex, national origin, disability status, genetics, protected veteran status, sexual orientation, gender identity or expression, or any other characteristic protected by federal, state, or local laws.