Remote Clinical Trial Monitoring Coordinator

Merck; Indianapolis (IN); Remote; USD 68,000 - 107,000; Full time

Benefits offered by this job

Annual bonus

Long-term incentive

Medical/dental/vision insurance

401(k) retirement plan

Job summary

Merck is seeking a Clinical Trial Coordinator-Monitoring to support site management, data tracking, and regulatory submissions. You will collate documents, update CTMS, manage labeling and translations, and assist with CTRAs and payments while collaborating with local teams and finance.

The role offers remote work options with a comprehensive benefits package and opportunities to support global clinical trial operations.

Qualifications

• Bachelor’s degree or completed job training in office management, administration, finance or health care.
• Excellent English (verbal and written) and strong communication skills.
• Knowledge of Good Documentation Practices and ICH-GCP.

Responsibilities

• Coordinate trial and site activities and maintain study tools, databases, and trackers.
• Support preparation of submission packages for IRB/ERC and regulatory authorities.
• Manage budgets, CTRAs, and payments with finance.
• Prepare Investigator trial file binders and maintain document management systems.
• Plan and support investigator meetings and site visits.

Skills

Communication skills

Time management

Organizational skills

Multitasking

Problem solving

ICH-GCP knowledge

Team collaboration

Education

Bachelor's degree

Office management / administrative training

Tools

MS Office

Microsoft Excel

Clinical IT applications

Job description

Merck is seeking a Clinical Trial Coordinator-Monitoring to support site management, data tracking, and regulatory submissions. You will collate documents, update CTMS, manage labeling and translations, and assist with CTRAs and payments while collaborating with local teams and finance.

The role offers remote work options with a comprehensive benefits package and opportunities to support global clinical trial operations.