LABORATORY TECHNOLOGIST

Job Juncture

Hackettstown (NJ)

On-site

USD 70,000 - 90,000

Full time

9 days ago

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Job summary

Job Juncture is seeking a Laboratory Technologist with a strong background in Hematology and Coagulation to support clinical trials and R&D activities. Responsibilities include validating instruments, training staff, and ensuring study protocols meet timelines.

The role involves coordinating with service operations, managing reagents and instruments, and assisting with documentation and study start-up activities.

Qualifications

  • B.S. Medical Technology/Clinical Laboratory Science or equivalent from an accredited four-year college or university.
  • MT(ASCP) Certification or equivalent preferred.
  • Minimum five years experience in Hematology and Coagulation; experience with instrument validations and training lab staff.

Responsibilities

  • Assist in clinical trial design and execution and support R&D activities.
  • Verify technical conditions prior to study start and ensure proper logistical setup for studies.
  • Coordinate with service operations on reagents, instruments, specimens, and contract documents.
  • Ensure protocol requirements are understood to meet study timelines.
  • Work with NCRA for study follow-up and monitoring visits as defined by procedures.
  • Maintain data traceability and centralization across study records.
  • Support validation of new equipment and assist in study binder maintenance.
  • Prepare clinical trial documentation from the site perspective and assist with product launches.

Skills

Hematology
Coagulation
Instrument validation
Lab staff training

Education

B.S. Medical Technology/Clinical Laboratory Science

Tools

Laboratory instruments

Job description

  • 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 deveopment 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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