Remote Clinical Trial Coordinator (CTC)

Merck; Columbus (OH); Remote; USD 68,000 - 107,000; Full time

Benefits offered by this job

Health insurance

401(k)

Job summary

Merck & Co., Inc. in the United States seeks a Clinical Trial Coordinator/CTC support to oversee trial and site administration, manage documents, and support regulatory submissions.

The role coordinates with COM, CRM, CRA and finance teams to maintain CTRAs and payments. Responsibilities include tracking essential documents, updating CTMS, coordinating study tools and labeling, supporting IRB/ERC submissions, and ensuring site readiness and timely reporting.

Qualifications

• Bachelor’s degree or completed job training in relevant field.
• Experience with clinical trial documentation and regulatory processes.
• Strong MS Excel and MS Office skills.

Responsibilities

• Track essential documents and report safety and other updates.
• Update CTMS databases and trackers.
• Coordinate distribution of study tools and documents.
• Manage labeling requirements and translation changes with country teams.
• Prepare documents and correspondence for trials.
• Archive clinical documents (eTMF) and assist with reconciliation.
• Support IRB/ERC submissions and regulatory filings.

Skills

Clinical Document Management

Clinical Research

Clinical Trial Documentation

Clinical Trial Management

Clinical Trials Monitoring

Clinical Trials Operations

Clinical Trial Support

Customer-Focused

Microsoft Excel

Microsoft Office

ICH-GCP Knowledge

Negotiation Skills (CTCs)

Time Management

Communication

Education

Bachelor’s Degree

Tools

CTMS

Microsoft Excel

Microsoft Office

Job description

Merck & Co., Inc. in the United States seeks a Clinical Trial Coordinator/CTC support to oversee trial and site administration, manage documents, and support regulatory submissions.

The role coordinates with COM, CRM, CRA and finance teams to maintain CTRAs and payments. Responsibilities include tracking essential documents, updating CTMS, coordinating study tools and labeling, supporting IRB/ERC submissions, and ensuring site readiness and timely reporting.