Remote Clinical Trial Monitoring Coordinator

Merck & Co.; Rahway (NJ); Remote; USD 68,000 - 107,000; Full time

Benefits offered by this job

Medical, dental, vision benefits

401(k) and retirement benefits

Paid holidays and vacation

Job summary

Merck & Co. in Rahway, NJ is seeking a Clinical Trial Coordinator-Monitoring (CTC-M) to support trial, site administration, and regulatory submissions. You will help prepare, collate, and archive clinical documents, update CTMS trackers, and assist with CTRAs and payments with finance teams.

The role collaborates with COM, CRM and CRA, ensuring timely site-starts, IRB submissions, and adherence to Good Documentation Practices. Remote work is available with travel as needed.

Qualifications

• Fluent in local languages and proficient in English (verbal and written).
• Good understanding of global clinical research guidelines and ability to work within them.
• Hands-on knowledge of Good Documentation Practices.

Responsibilities

• Provide data tracking and reporting support within Site Management & Monitoring.
• Collate, distribute, ship, and archive study tools and documents (eTMF).
• Update CTMS trackers and manage clinical trial documentation.
• Coordinate clinical and non-clinical supply management with country roles.
• Prepare investigator trial file binders and obtain translations when needed.

Skills

Fluent English

MS Excel

Good IT skills

ICH-GCP knowledge

Time management

Project management

Education

Bachelor's degree

Tools

MS Office

Job description

Merck & Co. in Rahway, NJ is seeking a Clinical Trial Coordinator-Monitoring (CTC-M) to support trial, site administration, and regulatory submissions. You will help prepare, collate, and archive clinical documents, update CTMS trackers, and assist with CTRAs and payments with finance teams.

The role collaborates with COM, CRM and CRA, ensuring timely site-starts, IRB submissions, and adherence to Good Documentation Practices. Remote work is available with travel as needed.