Clinical Toxicology Certifying Scientist - 2nd Shift at LabCorp
Phoenix, AZ 85018, USA -
Full Time


Start Date

Immediate

Expiry Date

04 Dec, 25

Salary

0.0

Posted On

04 Sep, 25

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

Medical Technology, Information Systems, Biology, Regulatory Requirements, Chemistry, Overtime

Industry

Pharmaceuticals

Description

At Labcorp, we believe in the power of science to change lives. We are a leading global life sciences company that delivers answers for crucial health questions —because we know that knowledge has the potential to make life better for all. Through our unparalleled diagnostics and drug development capabilities, we provide insights and accelerate innovations that not only empower patients and providers but help medical, biotech, and pharmaceutical companies transform ideas into innovations. Here, you can join our more than 70,000 employees, serving clients in more than 100 countries, as we work together to make a real impact on people’s lives. Join us in our pursuit of answers.
Are you looking to embark on a new challenge? The possibilities are endless when start your career at Labcorp! We would love to discuss the exciting opportunities you will encounter when you join our team as a Certifying Scientist. In this position, you will work in a patient focused, fast paced, and inspiring environment. You will have a dynamic role in the fulfilment of Labcorp’s overall mission of “Improving Health, Improving Lives.”
As a Certifying Scientist for the Toxicology department, you will be responsible for reviewing, certifying and reporting results for patient samples in the pain management compliance testing program and all clinical toxicology tests. This position interacts with both internal and external clients on interpretation of results and issues arising from testing, and routinely consults with Laboratory Managers and Directors concerning results and client test management.
Work Schedule: Sunday - Thursday, 2:00pm – 10:30pm (Some Overtime is required)
Shift: 2nd, this opening qualifies for an additional shift differential
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. Casual, PRN & Part Time employees regularly scheduled to work less than 20 hours are eligible to participate in the 401(k) Plan only. For more detailed information, please click here.

JOB REQUIREMENTS:

  • Bachelor’s degree in Biology, Chemistry, Clinical Laboratory Science, Medical Technology or meet local regulatory requirements
  • Master’s degree or Ph.D. in a Chemical or Biological Science is a plus
  • 5 years of pertinent laboratory experience is required
  • Certifying Scientist or Toxicology experience is preferred
  • Prior chromatography and/or mass spectrometry experience is preferred
  • Excellent research and problem resolution skills
  • Comfortability working in high volume, fast paced environment
  • Proficient with computers; Familiarity with laboratory information systems are a plus
  • Ability to prioritize and manage multiple tasks at a given time
  • High level of attention detail along with strong communication and organizational skills
  • Flexibility to work overtime or other shifts depending on business needs
    If you’re looking for a career that offers opportunities for growth, continual development, professional challenge and the chance to make a real difference, apply today!

How To Apply:

Incase you would like to apply to this job directly from the source, please click here

Responsibilities
  • Review all test results for applicable screening and confirmatory testing methodologies, relevant Quality Control data and associated documentation; certify and release results; ensure that results meet quality standards
  • Apply QC practices and procedures to the review, interpretation and reporting of results and when applicable monitor chain-of-custody documentation
  • Take proper remedial action in response to test systems being out of control limits, detect aberrant results of quality control and takes appropriate action
  • Provide consultation and assistance to clients when technical, interpretive, and/or regulatory questions arise
  • Assist in training fellow certifying scientists and other LabCorp employees in the interpretation and reporting of results and applicable departmental processes
  • Advise/consult with laboratory technical staff regarding routine testing issues and practices
  • Assist in preparation of litigation packages and affidavits. Potential to provide testimony under subpoena
  • Assist in preparation for inspections and audits. Interact with inspectors and auditors when appropriate
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