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Laboratory Technologist

Full Time
Posted 10 months ago

Responsibilities include:

  • Support Physicians, Research Manager and Clinical Study Staff with study specific administrative tasks.
  • Supports laboratory activities related to laboratory testing (phlebotomy, specimen collection, computer order entry and specimen processing) to ensure accurate result reporting.
  • Consent potential participants in clinical trials.
  • Provide protection of sensitive health information, study data, and proprietary information.
  • Collect pertinent visit assessment details ensuring accuracy of all records connected with each research participant.
  • Assist in obtaining vital signs and electrocardiograms.
  • Obtain, process and ship laboratory specimens to central laboratories.
  • Provide professional input regarding subject visits, assessments, evaluations and determination of eligibility for study participation.
  • Assist with transcription/data entry and review of completed Source Documents and Case Report Forms (CRFs).
  • Complete all source documents, Case Report Forms (CRFs) and data entry into research management systems accurately and timely to assure compliance with study sponsors.
  • Respond to queries generated in Electronic Data Capture (EDC) systems.
  • Ensure compliance with study protocols and SOPs.
  • Coordinate pick-up of outgoing packages with appropriate vendors.
  • Prepare visit documents and ancillary supplies required for upcoming visits.
  • Provide input during team discussions and meetings.
  • Organize and assist with the maintenance of study logs.
  • Organize incoming faxes and participant binders.
  • Monitor temperature-controlled study products.
  • File study specific documents on a daily basis.
  • Work to create a positive work culture.
  • Perform other related duties incidental to the work described herein.

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