Clinical Trial Support Specialist

EVERSANA; Chesterfield (MO); On-site; USD 42,000 - 64,000; Full time

Job summary

EVERSANA is seeking a Clinical Trial Assistant to support clinical studies, maintain trial documentation, and coordinate with trial sites, coordinators, and patients while adhering to good clinical practices. The role involves regulatory compliance, record-keeping, and drug/device dispensing as needed.

The CTA will contribute to study quality, organise study materials, and assist in protocol-related data collection, with some travel expected.

Qualifications

• High School diploma or GED required.
• Prior healthcare or life sciences experience preferred.
• Excellent written and verbal communication skills.
• Meticulous attention to detail.

Responsibilities

• Monitor study activities for protocol compliance and regulatory polices.
• Maintain records of study activity, CRFs, dispensing and regulatory forms.
• Dispense drugs or devices and calculate dosages as needed.
• Prepare for quality audits conducted by sponsors or regulators.
• Coordinate site visits and respond to inquiries on data issues.
• Support protocol development and administrative tasks.

Skills

Teamwork

Communication

Attention to detail

Education

High School Diploma/GED

Pharmacy Technician Registration

Tools

MS Office

Excel

Word

PowerPoint

Job description

EVERSANA is seeking a Clinical Trial Assistant to support clinical studies, maintain trial documentation, and coordinate with trial sites, coordinators, and patients while adhering to good clinical practices. The role involves regulatory compliance, record-keeping, and drug/device dispensing as needed.

The CTA will contribute to study quality, organise study materials, and assist in protocol-related data collection, with some travel expected.