Quality Specialist (Clinical Research QC Reviewer)

Position Summary:

• You are responsible for conducting quality control reviews of participant visits and source documentation within the CRIO eSource system.
• You ensure clinical documentation is complete, accurate, protocol-compliant, and aligned with GCP and ALCOA principles.

Key Responsibilities:

• Review completed participant visits in the CRIO platform to verify protocol-required procedures and documentation.
• Identify missing documentation, inconsistencies, protocol deviations, and GCP concerns, and document findings in tracking systems.
• Collaborate with site personnel to communicate findings and support timely resolution.

Qualifications:

• You have an Associate's or Bachelor's degree in a healthcare or life sciences field, or equivalent clinical research experience.
• You have at least three years of clinical research experience as a CRC, Regulatory Specialist, or similar role.
• You have strong understanding of GCP, protocol compliance, source documentation standards, and ALCOA principles.