Clinical Trial Associate II (Contractor) - Remote

Overview

The Clinical Trial Associate (CTA) II is responsible for coordinating clinical operations activities and ensuring compliance with Good Clinical Practices and study procedures.

In Short

• 100% remote position requiring location in the United States.
• Coordinate clinical operations activities and interact with cross-functional teams.
• Collaborate with CROs, consultants, and clinical trial sites.
• Facilitate timely communication among team members and site staff.
• Track and manage regulatory documentation and study performance indicators.
• Participate in site start-up activities and document tracking systems.
• Assist with the review and editing of clinical documents.
• Responsible for scheduling meetings and drafting minutes.
• Requires a B.A/B.S. degree and 3+ years of clinical research experience.
• Contract position requiring 40 hours per week.

Requirements

• B.A/B.S. degree in a relevant field.
• 3+ years of clinical research experience.
• Knowledge of GCP, ICH, and FDA regulations.
• Strong organizational and interpersonal skills.
• Excellent written and oral communication skills.
• Ability to handle multiple tasks in a dynamic environment.
• Basic knowledge of drug development processes.
• Occasional travel may be required.

Benefits

• Flexible work environment.
• Opportunity to work with a dynamic team in the biopharmaceutical industry.
• Engagement in meaningful work contributing to public health.