Supervisor, Clinical Laboratory Operations Area

Required

• Regulatory responsibilities per Good Clinical Practices (GCP)
• Regulatory responsibilities per Good Laboratory Practices (GLP)
• Regulatory responsibilities of “Testing Personnel” for high complexity testing as defined by 42CFR493.1495
• All other duties as assigned
• Molecular biology skills (e.g. DNA Extraction, Purification, PCR, qPCR, next-generation DNA sequencing) and related technical knowledge.
• Experience working with human specimens (e.g. blood, tissues and/or cells) and biohazardous material.
• Strong communication and interpersonal skills, ability to collaborate across teams and disciplines.
• Bachelor’s or higher in medical technology or laboratory science from an accredited institution, OR:
• Bachelor’s or higher in one of the chemical or biological sciences from an accredited institution + 6 months of high-complexity molecular experience and/or training in a clinical laboratory (holding a CLIA Certificate of Compliance/Accreditation)
• Bachelor’s or higher in medical technology or laboratory science, chemical science, or biological science from an accredited institution.
• Minimum of 1 year of experience and/or training in a clinical laboratory (holding a CLIA Certificate of Compliance/Accreditation) meeting the definition of “high-complexity”.
• Minimum of 3 years of pertinent molecular laboratory experience.