Clinical Trial Assistant (Medical Research)

TL;DR

Clinical Trial Assistant (Medical Research): Supporting clinical trials by maintaining organized files and performing pharmacy technician duties with an accent on regulatory compliance and trial site communication. Focus on managing drug dispensation records, ensuring adherence to study protocols, and coordinating logistical support for medical device trials.

Location: Must be based in Chesterfield, MO, USA

Company

A global commercialization services provider for the life sciences industry with over 7,000 employees dedicated to bringing innovative therapies to market.

What you will do

• Monitor study activities to ensure compliance with protocols and local, federal, and state regulatory policies.
• Maintain essential records including case report forms, drug dispensation records, and regulatory forms.
• Order, dispense, and calculate dosages for medical devices or drugs used in trials.
• Coordinate site visits and communicate with sponsors to resolve data gaps or protocol issues.
• Participate in quality assurance audits conducted by sponsors or federal agencies.
• Assist in the development of study protocols and data collection guidelines.

Requirements

• High School Diploma or GED.
• Current State of Missouri Pharmacy Technician Registration required.
• Prior work experience in healthcare or life sciences; clinical trial experience is preferred.
• Strong proficiency in MS Office programs (Excel, Word, PowerPoint).
• Excellent written and verbal communication skills.
• Ability to work onsite in Chesterfield, MO.

Culture & Benefits

• Certified Great Place to Work with a strong focus on diversity, equity, and inclusion.
• Competitive salaries and a comprehensive benefits package.
• Empowerment-driven culture emphasizing talent growth and continuous professional development.
• Collaborative global environment focused on improving patient lives.