Remote Senior Clinical Trial Coordinator & Process SME

Merck; Dover (DE); Remote; USD 74,000 - 118,000; Full time

Job summary

Merck & Co., Inc. in the United States seeks a Clinical Trial Coordinator to manage trial and site administration, document control, and regulatory submissions.

You will ensure timely maintenance of tracking tools, support IRB/ERC submissions, and collaborate with finance on CTRAs and payments. You will mentor junior CTCs, drive process improvements, and maintain Good Documentation Practices while coordinating with site staff and investigators.

Qualifications

• Minimum 3 years in Clinical Research or relevant healthcare experience.
• Completed job training (office management, administration, finance, health care preferred) or Bachelor’s Degree.

Responsibilities

• Track essential documents and report safety events.
• Update CTMS and trackers; collate and archive clinical documents.
• Support budgeting, CTRAs and payments with finance; ensure documentation compliance.
• Prepare submission packages for IRB/ERC and regulatory submissions.

Skills

Clinical Research

CTA

GCDMP

Microsoft Excel

Time Management

Training Delivery

Microsoft Office

Clinical Trial Management

Education

Bachelor's Degree

Tools

CTMS

Job description

Merck & Co., Inc. in the United States seeks a Clinical Trial Coordinator to manage trial and site administration, document control, and regulatory submissions.

You will ensure timely maintenance of tracking tools, support IRB/ERC submissions, and collaborate with finance on CTRAs and payments. You will mentor junior CTCs, drive process improvements, and maintain Good Documentation Practices while coordinating with site staff and investigators.