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Laboratory Assistant jobs in Alberta

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    • Ensure investigational product (IP), laboratory kits, and ancillary supplies are ordered, received, and inventoried.
    • Sponsor‑requested summaries and reports.
    • Pass all required laboratory training.
    • Maintain all laboratory equipment and be able to troubleshoot any problems, taking corrective action when necessary.
    • Experience in a chemical or mechanical testing laboratory.
    • Diploma in Engineering Technology (or equivalent).
    • Attention to detail; Strong work ethic.
    • Basic laboratory or quality-related experience.
    • Follow laboratory procedures and contribute to process improvements.
    • This is a full-time, temporary position.
    • Following direction of laboratory work orders/instructions and providing results in a timely manner.
    • Hands-on work experience required; previous experience in a…
    • View all Acuren Inspection, Inc. jobs - Calgary jobs - Laboratory Technician jobs in Calgary, AB
    • Salary Search: Lab Technician Level 1 (Temp Contract) salaries in Calgary, AB
    • See popular questions & answers about Acuren Inspection, Inc.
    • Following direction of laboratory work orders/instructions and providing results in a timely manner.
    • Hands-on work experience required; previous experience in a…
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    • Our mobile division provides services to insurance applicants, participants in wellness programs and private patients.
    • Paid mileage and tax deductions.
  • View similar jobs with this employer
    • Completion of core laboratory related courses or one year of recent, related experience within the last six years in the core laboratory section of the…
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    • Our mobile division provides services to insurance applicants, participants in wellness programs and private patients.
    • Paid mileage and tax deductions.
    • Use hand tools and laboratory equipment safely and accurately.
    • Inventory laboratory supplies and communicate supply needs to the appropriate team member.
    • This position will primarily be responsible for the preparation of seed samples for analysis and other miscellaneous laboratory assistant duties in support of…
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    • General laboratory clean-up and maintenance;
    • Knowledge from high school science courses and/or basic laboratory safety is an asset;
    • QC review of peer data;
    • Operate and maintain all laboratory equipment and inventory.
    • Perform and act as a backfill on entry-level laboratory tasks.
    • Maintain and calibrate laboratory equipment.
    • This role is responsible for responsible for conducting laboratory testing and analysis, documenting results, and…
    • Evaluate and initiate problem solving in all areas of the laboratory.
    • Monitor the laboratory to improve efficiencies and reduce costs in a continuous and…
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Job Post Details

Clinical Research Coordinator - job post

M.A.G.I.C. Clinic LTD
Calgary, AB T2E 7H7
$26–$29 an hour - Full-time

Job details

Pay

  • $26–$29 an hour

Job type

  • Full-time

Location

Calgary, AB T2E 7H7

Benefits

Pulled from the full job description

  • Paid time off
  • Dental care
  • Employee assistance program
  • On-site gym
  • On-site parking

Full job description

Company Overview
M.A.G.I.C. Clinic LTD is dedicated to advancing the diagnosis and management of rare genetic and metabolic diseases through innovative research and clinical care. Founded by a seasoned expert in the field, the clinic combines cutting-edge research with patient-centered services to improve outcomes for individuals with complex genetic conditions.

Overview
MAGIC Clinic is seeking a Clinical Research Coordinator to support the conduct of industry‑sponsored and investigator‑initiated clinical trials. This role combines hands‑on study coordination and regulatory‑compliant trial execution.

Key Responsibilities

Study Start‑Up & Regulatory

  • Assist with the review of clinical trial protocols to assess site feasibility.
  • Prepare, submit, and maintain regulatory documents for sponsors, CROs, and Research Ethics Boards (REB), including HREBA submissions.
  • Support site initiation activities, including staff training, study documentation, and site regulatory readiness.
  • Coordinate with procurement, finance, and vendors to ensure all study‑related services and contracts are in place.

Participant Management & Visit Coordination

  • Screen and identify potential participants in accordance with inclusion and exclusion criteria.
  • Ensure informed consent is obtained and maintained in compliance with REB and protocol requirements.
  • Coordinate patient visits, monitoring visits, audits, and site activities with the clinic administration team.
  • Ensure investigational product (IP), laboratory kits, and ancillary supplies are ordered, received, and inventoried.
  • Work closely with nursing staff, pharmacists, and investigators to ensure visits are conducted accurately and efficiently.

Data Management, Analysis & Publications

  • Perform detailed data entry, data cleaning, and query resolution within electronic data capture (EDC) systems.
  • Collaborate with monitors, data managers, and sponsors to resolve discrepancies in a timely manner.
  • Sponsor‑requested summaries and reports
  • Support data preparation for study close‑out, audits, and long‑term archiving.
  • Maintain high standards of data quality, completeness, and traceability.

Monitoring, Compliance & Quality

  • Support site monitoring visits and inspections.
  • Ensure studies are conducted in compliance with ICH‑GCP, Health Canada Division 5, and applicable privacy legislation (PIPA).
  • Assist with responding to audit findings and implementing corrective actions as needed.
  • Ensure all protocol amendments, Investigator’s Brochure (IB) updates, and study staff trainings are documented.

Qualifications & Experience

Required

  • Minimum 3–5 years of experience in clinical research coordination within Canada.
  • Experience working under Health Canada regulations and Canadian REBs.
  • Excellent written and verbal English communication skills.
  • Strong attention to detail with the ability to manage multiple studies simultaneously.
  • Proficiency with clinical trial systems (e.g., EDC platforms, IVRS/IWRS, SiteCentric).
  • Strong organizational and interpersonal skills; ability to work independently and collaboratively.

Preferred

  • CCRP or SOCRA certification.
  • Experience supporting publications, abstracts, or poster presentations.
  • Working knowledge of basic statistical analysis and research reporting.
  • Experience with industry‑sponsored trials and CRO interactions.

Why Join MAGIC Clinic?

  • Supportive environment focused on learning, professional development, and autonomy
  • Exposure to a wide range of clinical trials and therapeutic areas
  • A collaborative team committed to ethical, high‑quality clinical research

If you’re a motivated Clinical Research Coordinator looking to work in a dynamic clinical research setting, we’d love to hear from you.

Pay: $26.00-$29.00 per hour

Benefits:

  • Dental care
  • Employee assistance program
  • On-site gym
  • On-site parking
  • Paid time off

Application question(s):

  • Have you submitted any Ethics (IRB) Application
  • Do you have experience in Clinical Trials?

Licence/Certification:

  • GCP Certification (required)

Location:

  • Calgary, AB T2E 7H7 (required)

Work Location: In person

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