Specialist, Research Quality Assurance - FT - Days - MHS

What you’d do

Schedules and conducts audits of research protocols for non-compliance and high-risk studies, verifies source data, and reports findings to investigators and leadership. Full-time day shift role that also develops training materials for research staff. Found on the employer's careers page on Oct 12, 2026. Apply through the link.

You’ll need

• Experience auditing clinical research protocols
• Knowledge of SOPs and regulatory requirements
• Source data verification skills
• Experience with corrective and preventive actions
• Full-time day shift availability