Clinical Trials Quality Assurance Associate (Night)

• Perform ongoing quality checks to ensure data accuracy and compliance with SOPs, protocols, GCP, and regulatory requirements.
• Build eSource templates tailored to study protocols and ensure standardization.
• Enter and verify data in Electronic Data Capture (EDC) systems.
• Identify and document errors or deviations; support resolution and continuous quality improvement.
• Help generate quality reports and support risk assessments in collaboration with the clinical team.
• Contribute to CAPA development and share quality learnings across protocols/programs.
• Review key study documents for consistency and regulatory readiness.
• Assist in inspection preparation and support internal quality reviews.
• Resolve queries and prepare study-specific documentation and questionnaires.
• Participate in QA projects and support cross-functional teams as needed.

• Medical or clinical background (Pharm-D, MBBS, BDS strongly preferred).
• Familiarity with FDA, GCP, ICH guidelines and IRB processes.
• 1+ year experience in QA/QC or clinical research preferred.
• Proficient in documentation, data systems, and basic regulatory concepts.
• Detail-oriented with strong communication and time management skills.
• Able to work effectively in a fast-paced, collaborative environment.
• Knowledge of HIPAA and data privacy in clinical settings.

• Competitive salary and performance-based bonuses.
• Medical health insurance coverage.
• Employees Old-age benefits coverage.
• Professional learning and development support.
• Generous vacation and paid time off.
• Employee assistance programs for mental health.
• Company-sponsored events and team-building activities.
• Diverse, professional, and inclusive work environment.
• Opportunities for career growth.
• Cutting-edge technology and tools.
• Family-friendly policies, including parental leave.
• Commuter benefits or transportation assistance.
• Social responsibility and community involvement programs.

Minerva Research Solutions