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The Quality Control Associate reviews and validates clinical trial data to ensure compliance with protocols and regulatory guidelines, identifies errors, and assists in scheduling appointments.

The QC Reviewer is responsible for ensuring accurate quality control of laboratory data and documentation while adhering to SOPs and regulatory requirements.

The Manager oversees the Clinical Monitoring team, ensuring effective performance, quality control, training, and resource allocation for clinical trials.

The Study Design Specialist reviews study protocols and creates study designs in Watson LIMS, manages sample discrepancies, and generates reports while ensuring compliance with industry standards.