Quality Assurance Associate (Clinical Trial) – Evening Shift

About the role

Minerva Research Solutions is seeking a Quality Assurance Associate to support clinical trial data integrity during the evening shift. The role focuses on monitoring data quality, ensuring compliance with FDA, GCP and sponsor protocols, and maintaining inspection readiness.

Key responsibilities

• Perform data‑driven quality monitoring activities to verify compliance with regulatory requirements, SOPs and inspection readiness.
• Conduct quality control checks, identify source documentation errors and track non‑conformances.
• Prepare periodic quality reports, assess risk areas with clinical teams and develop mitigation plans.
• Collaborate on audit/inspection observations, implement corrective action plans (CAPAs) and support internal and sponsor audits.
• Review key trial documents for regulatory submission and assist cross‑functional workgroups in resolving compliance matters.

Required profile

• Fresh MBBS graduate with strong interest in clinical research.
• Knowledge of FDA, GCP, ICH, IRB requirements and HIPAA privacy regulations.
• Understanding of clinical trial lifecycle and documentation standards.
• Excellent communication, attention to detail and ability to manage multiple tasks in a fast‑moving environment.

What we offer

• Competitive salary with performance‑based bonuses.
• Medical health insurance and old‑age benefits.
• Flexible work hours, remote options and night‑shift allowance.
• Professional development, generous vacation and paid time off.
• Inclusive workplace, career growth opportunities and family‑friendly policies.