The Pathologist Director is accountable for -
? Responsible for routine microscopic review and interpretation based on slide/image examination to support AP production, validation and quality management activities in a timely manner.
? Major duties involves, but not limit to, histopathologic, immunohistochemical and morphological evaluation and report; microscopic preparation of slide for downstream molecular pathology analysis as needed.
? Participates in compliance-driven activities related to AP service as needed , including but not limit to external audit/inspection from client, regulatory and accreditation organization as well as internal audit for this purpose.
? Participate in all the internal/external training or continuous education which pertains to microscopic examination and interpretation.
? Communicate the significance of pathological findings to manager, PM and other related individuals.
? Provide consultations about the medical significance of AP laboratory data. Interpret, correlate and communicate laboratory data to clinical trial sponsors.
? Perform testing and quality control procedures as per LabCorp Clinical Trials Quality Assurance guidelines.
? Provide consultations to ensure preparations of the tissue samples maintain high quality standards.
? Assist in all quality control and quality assurance programs for anatomic pathology.
? Comply with all safety regulations and policies as they relate to the laboratory environment.
? Ensure all biohazardous waste is handled in a manner that complies with Covance Central Laboratories safety and environmental policies.
