Toronto, Ontario – Clinical Research Technician

Position Reports to: Senior Manager, Clinical Operations

Duties and Responsibilities:

  • Review study protocol and participate in the protocol training meeting prior to performing any study related activities.
  • Perform ECG and vitals
  • Compliance check on subjects
  • Collect/process blood and urine samples as well as other specimens as required.
  • Perform drug/cotinine screen and alcohol test as well as urine pregnancy test.
  • Obtain body measurements including height and body weight, and calculate Body Mass Index (BMI).
  • Catheter insertion and removal
  • Proper collecting, handling and processing of PK samples
  • Process and ship lab samples
  • Assist in drug administration by performing hand and mouth check
  • Serve and/or monitor meals
  • Maintain accurate, complete, legible and timely data entry
  • Perform screening reception duties as required, including but not limited to ID verification, recording of Demographic information (Medical Screening staff only).
  • Perform data review of the source and/or other related documents as required.
  • Write and/or review source documentation forms
  • Conduct clinical staff training
  • Performs other tasks and projects as assigned

Qualifications:

  • 2 year Medical Technology Diploma, or equivalent
  • 1-2 years work experience in a CRO (preferably in conducting Phase I /Bioequivalence clinical trials)
  • 1-2 years of recent phlebotomy and ECG experience
  • A minimum of 1 year experience in a basic laboratory setting
  • Flexible hours depending on business requirements.
  • Rotating shifts and weekend requirements

Please send your resume to resumes@biopharmaservices.com