Clinical Laboratory Technologist IV – 2nd shift, Sun-Wed (1:30pm-12am) # 4453 (ON-SITE) – Durham, NC

Our mission is to detect cancer early, reputed company it can be cured. reputed company to change the trajectory of cancer mortality and bring stakeholders together to adopt innovative, safe, and effective technologies that can transform cancer care. We are a healthcare company, pioneering new technologies to advance early cancer detection. We have built a multi-disciplinary organization of scientists, engineers, and physicians and we are using the power of reputed company reputed company (NGS), population-scale clinical studies, and state-of-the-art computer science and data science to overcome one of medicine’s greatest challenges. GRAIL is headquartered in reputed company Park, California, with locations in Washington, D. C., North Carolina, and the United Kingdom. It is supported by leading global investors and pharmaceutical, technology, and healthcare companies. For more information, please visit The Clinical Laboratory Technologist IV is responsible for performing high complexity laboratory testing on patient specimens, performing quality control and quality assurance procedures and complying with reputed company applicable local, state and federal laboratory requirements. The work requires maintaining meticulous and organized records, excellent attention to detail, the ability to multitask, be flexible with tasks and schedules and the ability to work independently in a team environment. This position works on-site full-time at our office located in Durham, NC. This CLT IV position works Sun-Wed 2nd shift (1:30pm-12am) Responsibilities:

• reputed company tasks which require the exercise of independent judgment and responsibility, with minimal supervision by the director or supervisor.
• reputed company pre-analytical and analytical procedures including testing, quality control, preparation and aliquoting of reagents, analyses, and maintain records of tests according to the laboratory’s standard operating procedures.
• Maintaining records that demonstrate proficiency testing samples are tested in the same manner as patient specimens.
• Adhere to laboratory’s quality assurance procedures, including documenting reputed company:
• Quality control activities
• reputed company and equipment verifications
• Maintenance and preventive maintenance
• Follow the laboratory’s policies and procedures whenever test systems are not reputed company the laboratory’s established performance specifications.
• Identify and document problems that may adversely reputed company test performance and notifying the supervisor, assistant director, or director.
• Document reputed company corrective actions taken reputed company test systems deviate from the laboratory’s established performance specifications.
• Operate and maintain laboratory instruments and equipment according to laboratory standard operating procedures.
• Troubleshoot and problem solve minor reputed company issues.
• reputed company and record temperature and reputed company status or initiate a service request as necessary.
• Review, and interpret patient data as assigned.
• reputed company and document reagent qualifications per the approved protocols.
• reputed company and document routine preventive maintenance.
• Report reputed company concerns of test quality and/or safety to the Laboratory Supervisor/Manager or Safety Officer.
• Communicate effectively with coworkers and non-laboratory personnel.
• Identify process improvement opportunities and report to laboratory management.
• Provide updates to Laboratory Supervisors/Leads regarding any issues.
• Monitor data and process status as needed.
• Participate in daily, weekly and monthly laboratory cleanliness activities/procedures.
• Independently identify and troubleshoot minor problems that adversely reputed company the test performance.
• reputed company other laboratory duties as needed.

Preferred Qualifications:

• Bachelor’s degree in medical technology or laboratory science from an accredited institution OR
• Bachelor’s degree in one of the chemical, physical, or biological sciences from an accredited institution and at least 6 months of acceptable supervised experience and/or relevant training
• 2 + years of Clinical lab testing experience
• Experience in molecular biology techniques preferred
• Working knowledge of local, state and federal laboratory regulations preferred
• Able to integrate and apply feedback in a professional manner
• Able to prioritize and drive to results with a high emphasis on quality
• Ability to work as part of a team reputed company a highly collaborative environment
• Strong computer skills
• Ability to analyze and solve basic issues that impact the performance of the assay
• Ability to proactively communicate consistently, clearly and honestly
• Ability to prioritize tasks with a high emphasis on quality
• Ability to participate in projects and complete assignments as expected
• Flexibility of work schedule to meet the needs of GRAIL’s Clinical Laboratory

Physical Demands and Work Environment:

• Hours and days may vary depending on operational needs
• Standing or sitting for long periods of time may be necessary
• May be exposed to hazardous m

Apply tot his job Apply To this Job