Clinical Research Monitor

Zachary Piper Solutions is seeking a Clinical Research Monitor to support a company focused on advancing FDA‑regulated medical product development. This position is hybrid at Ft. Detrick, Frederick, Maryland. The Clinical Research Monitor will conduct clinical trial monitoring, ensure regulatory compliance, and support fast‑paced clinical and regulatory operations. Join a mission‑driven team directly impacting the safety and effectiveness of lifesaving military medical solutions.

Responsibilities for the Clinical Research Monitor include:

• Develop Clinical Monitoring Plans for single‑site and multi‑center studies across domestic and international programs
• Conduct centralized and remote monitoring of electronic source documents, eCRFs, and study data
• Identify and mitigate clinical, safety, and data‑quality risks through trend and metric analysis
• Prepare and maintain Clinical Monitoring Reports and sponsor regulatory file documentation
• Review calibration/maintenance records and documentation for investigational product and sample shipments

Required Qualifications for the Clinical Research Monitor include:

• 4+ years of experience supporting clinical research
• Experience reviewing electronic source documents, eCRFs, and preparing Clinical Monitoring Reports
• Experience with remote data review, regulatory documentation, equipment calibration review, and shipment documentation
• Bachelor’s degree
• U.S. Citizenship with the ability to obtain a favorable NACLC T3 investigation

Compensation for the Clinical Research Monitor includes:

• Salary Range: $60,000-85,000 **depending on experience**
• Full Benefits Package: PTO, Paid Holidays, Medical, Dental, Vision, 401K, Tuition Reimbursement, Sick leave as required by law

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Keywords: clinical research monitor, clinical monitoring, eCRF, clinical operations, FDA, 21 CFR 312, ICH, remote monitoring, regulatory documentation, investigational product shipments, USAMRDC, ORA, medical research, calibration records, NACLC T3, Fort Detrick