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iLocatum

LABORATORY TECHNOLOGIST

Hackettstown, NJ · On-site

Laboratory Technologist Education Experience: B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required. MT(ASCP) Certification or ...

Centstone HC

Medical Laboratory Technologist

Tahlequah, OK · On-site

$1.5K - $1.6K/wk

Medical Laboratory Technologist Location: Cherokee Nation Region Pay Rate: $1500 TO $1680/ Week Contract: Contract Schedule: Night shift (9Pm To 7Am) Experience: Lab MT experience preferred About the ...

Vitrolife Group

Laboratory Technologist

Torrance, CA · On-site

$30 - $32/hr

Torrance, California Salary Range: $30 - $$32 / hr Position Summary We are currently seeking a Laboratory Technologist to join our Torrance-based team. This individual will play a key role in ...

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LABORATORY TECHNOLOGIST

Hackettstown, NJ • On-site

iLocatum
Executive Search Services • 1 - 10 employees
Learn more about iLocatumexternal

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Posted 19 days ago

Job description

Laboratory Technologist

Education Experience:

B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university required.

MT(ASCP) Certification or equivalent preferred.

Minimum five years experience in Hematology and Coagulation preferably, experience with instrument validations, correlations and training lab staff on new laboratory instrumentation.

Experience:

The Laboratory Technologist is involved with clinical trial regulations in order to provide input to clinical trial designs and execution. Assist in conducting and supporting R&D activities and clinical trials, in development of new Hematology and Hemostasis product launches. You will verify technical conditions prior to the start of a study. Working with members of the service operations team, create good logistical conditions for clinical studies, which include delivery of reagents and/or instrument, specimens, exchange of correspondence, contracts, and administrative documents. Additional duties & requirements include:

  • Ensure full understanding of the protocol requirements to ensure the study proceeds efficiently in order to meet organizational time lines.
  • Work closely with the NCRA for all necessary study follow-up in accordance with defined procedure, including but not limited to the checklist for site initiation and monitoring visits, etc.
  • Ensure corrective actions are followed for proper conduct to freeze databases of results in accordance with the studies initial objectives.
  • Check completeness of records (all forms of media: paper and electronic), ensure centralization and formatting of data from studies, as well as ensuring traceability of data.
  • Use knowledge and experience with instrument validation, interference, on-board stability, Limit of Blank, Limit of Detection, Limit of quantification to perform Linearity and Method Comparison testing.
  • Maintain laboratory equipment following daily, weekly and monthly maintenance schedules as well as required quality control for all laboratory analyzers.
  • Participates in validation of new equipment as appropriate.
  • Assist the NCRA's in the development and maintenance of clinical study binders and utilization of eCRF.
  • Manages the Laboratory equipment service contracts and documentary elements of clinical trial activities;
  • Completes necessary clinical trial documentation from the site's perspective, in preparation of study start up.
  • Give scientific presentations as required.
  • Offer support on new product launches as needed.

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