Remote Senior Clinical Trial Coordinator: Drive Study Ops

Merck; Rahway (NJ); Remote; USD 90,000 - 130,000; Full time

Benefits offered by this job

Remote work options

Job summary

Merck is seeking a Clinical Trial Coordinator/CTC to oversee trial and site administration, document management, budgeting, and meetings coordination. You will collaborate with COM, CRM, CRA, and finance to manage CTRAs, payments, and regulatory submissions.

The role requires 3+ years in clinical research, strong documentation practices, and proficient IT skills. Remote-ready in the US with travel expectations and a focus on process improvement.

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 (e.g., Safety Reports).
• Collate, distribute/ship, and archive clinical documents (eTMF).
• Maintain CTMS databases and trackers.
• Support clinical supply and non-clinical supply management with country teams.
• Assist with IRB/ERC submissions and regulatory packages.

Skills

Clinical Research

CTA (Clinical Trial Agreements)

GCDMP

Microsoft Excel

Microsoft Office

Time Management

Training Delivery

Leadership

Communication

Customer-Focused

Education

Bachelor’s Degree

Office management training / finance training

Tools

CTMS

eTMF

MS Office

Job description

Merck is seeking a Clinical Trial Coordinator/CTC to oversee trial and site administration, document management, budgeting, and meetings coordination. You will collaborate with COM, CRM, CRA, and finance to manage CTRAs, payments, and regulatory submissions.

The role requires 3+ years in clinical research, strong documentation practices, and proficient IT skills. Remote-ready in the US with travel expectations and a focus on process improvement.