Associate Clinical Director, Laboratory Services

Under the direction and mentorship of our Clinical Director, Global Laboratory Services, this position is responsible for providing effective clinical leadership for the development and delivery of global laboratory services and products. This position is responsible for clinical oversight of the North American Central Safety and Cellular Laboratory, assuring that operations are conducted in compliance with applicable regulations. What You'll Do • Laboratory Oversight & Administrative + Provide effective and efficient scientific direction and oversight for the CTI North American Central Safety and Cellular Laboratories + Ensure the development, implementation, and compliance of globalized standardized processes for the CTI Central Safety and Cellular Laboratories + Ensure that technical staff are qualified to perform all testing and have met training and/or competency requirements + Ensure all technical staff have current and up to date licensing and credentials + Delegate the responsibilities of the Laboratory Supervisor, Specialty Laboratory Directors/Supervisors, Quality Control Manager and Testing Personnel to employees who are qualified to perform such duties + Responsible for designing, validating, and maintaining accurate, precise and clinically useful laboratory tests to meet clients' needs + Monitor all work performed in the laboratory to ensure that clinically reliable data is generated and efficiently reported + Provide advice to sponsors and clients regarding the significance of laboratory findings and ensure that reports of test results include pertinent information required for specific patient/subject interpretation + Subject Matter Expert for client interactions and business development activities + Ensure that a supervisor provides onsite supervision of high complexity test performance + Act as clinical representative for regulatory interactions that include FDA/CLIA/CAP/EMA/ISO, etc + Oversee and maintain relevant laboratory testing and reporting, laboratory and clinical trial files and other laboratory documentation to ensure inspection readiness at all times + Lead the development and continuous improvement of laboratory SOPs, and GLPs and provide oversight of laboratory quality & adherence to established processes and plans + Review and approve laboratory documentation such as policies and procedures, validation plans and reports, training and competency assessments, and reagent/control/instrument qualifications, quality audits, deviation approval requests, and nonconforming event reports + Maintain an effective working relationship with applicable accrediting and regulatory agencies + Participate in the selection of partner laboratories + Report all concerns of test quality and/or safety to Clinical Director, Global Laboratory Services • Labora...