Clinical Technologist Trainee LCMS Instrument​/Data Analysis

Overview

Med Tox Laboratories is a subsidiary of Laboratory Corporation of America (Lab Corp). The integration of Lab Corp and Covance in 2015 makes Lab Corp the largest health care diagnostic company in the world. Lab Corp operates in over 60 countries creating opportunities for career growth and advancement. This position is for a Clinical Medical Monitoring LCMS / Data Review Technologist Trainee in the Clinical Tox Assure Laboratory, performing high complexity testing for pain management in urine samples and handling instrumentation/data analysis for multiple LCMS/MS methods.

This bench uses 40+ LC-MS/MS instrument platforms and a cloud-based processing platform (Ascent).

Pay Range: 21.00 - 23.00 per hour

All job offers are based on candidate skills and prior relevant experience, applicable degrees/certifications, as well as internal equity and market data.

Work Schedule: Mon/Tues/Fri/Sat 7:00am - 5:30pm

Shift: 1st

Benefits: Employees regularly scheduled to work 20 or more hours per week are eligible for comprehensive benefits including Medical, Dental, Vision, Life, STD/LTD, 401(k), Paid Time Off (PTO) or Flexible Time Off (FTO), Tuition Reimbursement and Employee Stock Purchase Plan. Part-time/PRN employees may participate in 401(k) per plan terms. For more information, please refer to internal policy documents.

The following duties reflect key responsibilities. Other duties may be assigned.

• Work with LC-MS/MS instrumentation utilizing a cloud-based processing platform, Ascent.
• Receive extracted specimens for testing; evaluate batches and test orders; determine priority of work to maintain acceptable turnaround time.
• Perform large amounts of daily electronic data analysis on computer stations outside of the laboratory.
• Recognize unacceptable or unusual specimens within a batch or set and handle appropriately.
• Adhere to SOPs while performing data analysis on patient and proficiency samples as well as calibration, quality control and blank samples.
• Evaluate raw and final data for accuracy; recognize and correct errors; interpret results to produce a final report.
• Follow quality control rules; monitor controls/calibration for error detection within a batch and take corrective action as needed.
• Maintain, calibrate and clean instrumentation and work area; perform scheduled maintenance and critical function checks; troubleshoot as indicated.
• Maintain accurate records and documentation for all laboratory tests and equipment including logs and SOPs.
• Proactively monitor assay and instrument performance to prevent downtime and delays in reporting results.
• Prepare and use laboratory reagents, standards and quality controls according to SOPs and time frames.
• Apply Good Documentation Practices (GDP) in all documentation.
• Deliver accurate, high-quality patient care while maintaining efficiency.
• Participate in instruction and training of others; demonstrate and/or explain the testing process to others or observe testing performed by others.

• Bachelor’s degree in Chemical or Biological Science, Clinical Laboratory Science, Medical Technology or meet local regulatory (CLIA & State) requirements.
• Previous experience is not required.
• Proven ability to prioritize tasks and manage time.
• Excellent research and problem resolution skills.
• Ability to work effectively in a fast-paced production environment to meet turnaround times.
• High accuracy and attention to detail.
• Good written and verbal communication skills and interpersonal skills.
• Able to work independently within a team under general supervision.
• Some overtime may be required depending on departmental needs.

Labcorp is an Equal Opportunity Employer. We encourage all to apply. If you need assistance or accommodation, please contact Labcorp.