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Clinical Research Assistant

  • Hamilton, ON, Canada

$27 to $32 CAD / hour · Full-time

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Job details

Pay
$27 to $32 CAD / hour
Job type
Full-time
Apply by
Experience
$27 to $32 an hour, based on experience.
Working hours
40 hours a week
Posting language
English
Posted

Original job description

We’re hiring our first Clinical Research Assistant. You’ll own the lab bench, the investigational product and the data entry across every study, so our coordinators can spend their day with participants.

Hamilton Medical Research Group (HMRG) is a clinical research site in Hamilton. We run Phase II to IV drug trials for global pharmaceutical sponsors in cardiovascular disease, diabetes, obesity, respiratory, renal and vaccine research, with a small team of coordinators and physicians led by Dr. Richard Tytus.

What you’ll do

  • Receive investigational product: check it against the packing list and temperature record, confirm receipt in the sponsor’s IRT, store it, and keep accountability logs ready for the monitor.
  • Be the second check on investigational product when a protocol or pharmacy manual calls for one.
  • Process blood and urine samples exactly as the lab manual says: spin, separate, aliquot, label and freeze.
  • Pack and ship ambient, refrigerated and frozen (dry ice) samples, book couriers and track every box to the central lab.
  • Keep lab kits and shipping supplies stocked and in date.
  • Enter visit data into sponsor EDC systems and help close queries.
  • Take vital signs and ECGs, and draw blood if you’re certified.

What you bring

  • 2+ years of hands-on work with patients or clinical samples, ideally at a clinical research site on industry-sponsored drug trials.
  • Hands-on experience collecting, processing or shipping samples, ideally to a central lab manual.
  • Data entry in a sponsor EDC system (for example Medidata Rave, Veeva or InForm).
  • Current GCP training and TDG/IATA certification for Category B specimens and dry ice. If yours has lapsed, we’ll get you recertified.
  • A plus: receiving investigational product in an IRT and keeping accountability logs, and phlebotomy certification.
  • Care with detail. You catch the wrong tube or kit number before it leaves the building.

What we offer

  • $27 to $32 an hour, based on experience.
  • 40 hours a week, Monday to Friday, 8:00 to 4:30, with the occasional early start for a fasting visit.
  • Group benefits from your first day.
  • A $100 monthly transportation stipend.
  • Paid time for training and certification.
  • A path to Clinical Research Coordinator.

This posting is for an existing vacancy. We’ll let everyone we interview know the outcome within 45 days of their last interview.

More about this job

Responsibilities

The Clinical Research Assistant at Hamilton Medical Research Group will receive and store trial drugs, process and ship blood and urine samples, and enter visit data into sponsor systems. The role also takes vital signs and ECGs and keeps lab supplies stocked.

Requirements

Candidates need 2+ years of hands-on work with patients or clinical samples, ideally on industry-sponsored drug trials, plus current GCP training and TDG/IATA certification. Sponsor EDC data entry experience and careful attention to detail are required.

Skills

  • Investigational product management
  • IRT (Interactive Response Technology)
  • Sample processing (centrifugation, aliquoting, labelling, fr
  • Sample packing and shipping
  • Dry ice handling
  • TDG and IATA shipping compliance
  • Good Clinical Practice (GCP)
  • EDC data entry
  • Medidata Rave
  • Veeva
  • InForm
  • Query resolution
  • Vital signs measurement
  • ECG acquisition
  • Phlebotomy
  • Inventory and supply management
  • Accountability logging
  • Attention to detail
  • Protocol and lab manual adherence
  • Courier booking and shipment tracking

Benefits

  • Transportation stipend
  • Paid training and certification
  • Career path

Categories

  • Healthcare
  • Science & Research
  • Administrative

Keywords

  • clinical research assistant
  • clinical trials
  • Phase II
  • Phase III
  • Phase IV
  • investigational product
  • IRT
  • accountability logs
  • sample processing
  • sample shipping
  • dry ice
  • TDG
  • IATA
  • GCP
  • EDC data entry
  • Medidata Rave
  • Veeva
  • InForm
  • phlebotomy
  • ECG

Seniority

Mid level

Perks

  • Transit support
  • Paid training
  • Remote work allowance

Licences and certifications

  • GCP
  • TDG
  • IATA
  • Phlebotomy certification

Tools

  • Medidata Rave
  • Veeva
  • InForm
  • IRT
  • dry ice

Languages

  • English

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