Remote Senior Clinical Trial Coordinator

Merck & Co., Inc; United States; Remote; USD 74,000 - 118,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

401(k)

Job summary

Merck & Co., Inc. invites applications for a Clinical Trials Coordinator responsible for trial and site administration, document management, and regulatory submissions. You will collaborate with cross-functional teams, maintain CTMS/eTMF accuracy, and support budgeting and payments to investigators.

The role emphasizes process SME responsibilities, training junior staff, and continuous improvement within a global clinical operations context. Experience in GCP and CRM tools is preferred.

Qualifications

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

Responsibilities

• Track essential documents and report safety reports.
• Collate, distribute and archive clinical documents (eTMF).
• Update CTMS and trackers.
• Support budgeting, CTRAs and payments with finance team.
• Coordinate submission packages for IRB/ERC and regulatory submissions.
• Organize meetings and support local investigator meetings.
• Mentor junior CTCs and share best practices.

Skills

Clinical Research

CTA

Clinical Trial Management

GCDMP

Time Management

Microsoft Excel

Microsoft Office

Negotiation

Education

Bachelor's Degree

Tools

CTMS

eTMF

Job description

Merck & Co., Inc. invites applications for a Clinical Trials Coordinator responsible for trial and site administration, document management, and regulatory submissions. You will collaborate with cross-functional teams, maintain CTMS/eTMF accuracy, and support budgeting and payments to investigators.

The role emphasizes process SME responsibilities, training junior staff, and continuous improvement within a global clinical operations context. Experience in GCP and CRM tools is preferred.