Laboratory Technologist

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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