Remote Clinical Trials Coordinator

Ergclinical; Northern (KY); Hybrid; USD 45,000 - 75,000; Full time

Job summary

Ergclinical is seeking a Clinical Trials Assistant (CTA) for a remote, full-time position in the CRO sector. The role supports Clinical Operations to ensure studies are completed on time, within budget, and compliant with SOPs and FDA/ICH guidelines.

You will archive trial master files, prepare regulatory documents, and assist with study drug release and investigator meetings. The candidate should have a BS/BA (or equivalent) and at least 2 years of clinical research exposure, with strong

Qualifications

• BS/BA preferred; high school diploma or equivalent accepted with relevant experience.
• General knowledge of clinical research requirements including GCP and ICH guidelines.
• Minimum of 2 years of clinical research experience; CTA experience preferred but not required.

Responsibilities

• Assist in preparing regulatory documents, study binders, templates, and communications.
• Assist with study drug release processes and regulatory packet review.
• Develop study-specific training materials and help plan investigator meetings.
• Interact with sites to respond to issues and manage shipments as needed.
• Monitor and track monitoring visit reports and study progress.
• Assist with study data review at CRF, data listing, and tables.

Skills

Strong communication

Time management

Attention to detail

Multitasking

Teamwork

Education

BS/BA preferred

Job description

Ergclinical is seeking a Clinical Trials Assistant (CTA) for a remote, full-time position in the CRO sector. The role supports Clinical Operations to ensure studies are completed on time, within budget, and compliant with SOPs and FDA/ICH guidelines.

You will archive trial master files, prepare regulatory documents, and assist with study drug release and investigator meetings. The candidate should have a BS/BA (or equivalent) and at least 2 years of clinical research exposure, with strong