Remote Clinical Trial Coordinator - Site & Docs Lead

Merck; Lincoln (NE); Remote; USD 68,000 - 107,000; Full time

Benefits offered by this job

Medical/Dental/Vision benefits

401(k) retirement plan

Paid holidays and vacation

Job summary

Merck & Co., Inc. is seeking a Clinical Trial Coordinator for Lincoln, NE area to oversee trial and site administration, and manage document control in line with GCP guidelines.

You will collaborate with investigators, COM, CRM and CRA, while supporting CTRAs and payments in a dynamic, remote-friendly environment. A Bachelor’s Degree or equivalent and strong MS Excel/Office skills are required.

Qualifications

• Completed job training in office management, administration, finance, or health care preferred or a Bachelor’s Degree.
• Experience in clinical trial documentation and regulatory processes is preferred.
• Proficient in MS Excel and MS Office; strong IT skills.

Responsibilities

• Trial and site administration tasks including tracking essential documents and safety reports.
• Document management: collate, distribute/ship, archive clinical documents and assist with eTMF reconciliation.
• Regulatory & site start-up support including IRB/ERC submissions and regulatory submissions.

Skills

Clinical Document Management

Clinical Research

Clinical Trial Documentation

Clinical Trial Management

Clinical Trials Monitoring

Clinical Trials Operations

Clinical Trial Support

Customer-Focused

Microsoft Excel

Microsoft Office

Education

Bachelor’s Degree or equivalent

Job description

Merck & Co., Inc. is seeking a Clinical Trial Coordinator for Lincoln, NE area to oversee trial and site administration, and manage document control in line with GCP guidelines.

You will collaborate with investigators, COM, CRM and CRA, while supporting CTRAs and payments in a dynamic, remote-friendly environment. A Bachelor’s Degree or equivalent and strong MS Excel/Office skills are required.