Clinical Trial Associate II - Remote

Overview

The Clinical Trial Associate II will support the Director of Clinical Operations in managing clinical trials, ensuring compliance with protocols and regulations, while contributing to the advancement of novel therapies for obesity and related conditions.

In Short

• Provide support for clinical trial management activities.
• Assist in documentation preparation according to GCP requirements.
• Track clinical trial progress and metrics.
• Ensure compliance with study protocols.
• Organize study files and documentation.
• Communicate with vendors and internal teams.
• Participate in training for CRO teams and staff.
• Maintain accurate records of trial materials.
• Perform additional duties as assigned.

Requirements

• Basic understanding of ICH GCP regulations.
• Ability to multi-task effectively.
• Strong communication and organizational skills.
• 2+ years of experience in a relevant field.
• Proficient in Microsoft Office.
• Interest in clinical trials and research.

Benefits

• Comprehensive health benefits.
• Flexible time off and paid holidays.
• Monthly wellness stipend.
• Generous 401(k) match.
• Disability and life insurance.