Clinical Research Associate - Remote

Overview

The Clinical Research Associate plays a vital role in the Clinical Operations team, ensuring the success of clinical trial operations and management through various responsibilities.

In Short

• Monitor clinical studies of investigational and approved products.
• Manage and train site personnel on protocol requirements.
• Handle investigational supplies at individual sites.
• Document investigational product dispensing and inventory.
• Monitor trial enrollment and report on updates.
• Review source data for accuracy and integrity.
• Resolve data discrepancies with study centers.
• Review regulatory documentation for accuracy.
• Maintain consistent contact with study centers and personnel.
• Follow Good Documentation Practices.

Requirements

• Bachelor's or advanced degree in biological sciences or related field.
• 2 years of prior experience as a Clinical Research Associate preferred.
• Detail oriented with excellent organizational skills.
• Strong interpersonal and communication skills.
• Flexibility with changing priorities.
• Ability to prioritize multiple tasks efficiently.
• Familiarity with medical and pharmaceutical terminology.
• Extensive knowledge of FDA regulations.
• Ability to travel on short notice.
• Proficiency in Microsoft Word, Excel, and PowerPoint.

Benefits

• Full medical, dental, and vision insurance options.
• Flexible PTO for personal and professional needs.
• 401(k) plan with company match.
• Support for skill expansion and career growth.
• A collaborative and supportive work environment.