Lab Technician Job Description Samples

Lab Technician Job Description 1:

Job Summary:
•Assists with the conduct of clinical trials through the collection of biological samples, performing venipuncture, electrocardiograms, tube labeling, sample processing, and other related tasks in accordance with Protocol, Good Clinical Practice, Standard Operating Procedures and relevant regulatory guidelines
Core Responsibilities:
•Collects, processes and stores biological samples as per Protocol and safety guidelines
•Assists in preparation of labels, labeling tubes and setup for study conduct
•Performs electrocardiograms
•Performs Protocol specific tests within specified timelines
•Maintains a clean, safe work environment
•Maintains the equipment, ensuring that calibration and maintenance are completed within appropriate time frames
•Assists with monitoring and maintenance of applicable equipment
•Performs shipping and handling of samples as per protocol requirements and IATA guidelines
•Assists with Clinic Attendant duties as required
•Ensures that biological specimens are disposed of appropriately
•Other duties as assigned

Skills & Attributes:
•Ability to work independently and as a team player
•Ability to organize and prioritize within a changing environment
•Ability to work different shifts (weekends, evenings, nights)
•Demonstrates initiative and attention to detail
•Uses safety/universal precautions to protect self, subjects and staff
•Able to appropriately implement Protocol and regulatory requirements in study conduct
•Proficient in venipuncture, centrifugation, sample storage and performing electrocardiogram
•Excellent interpersonal and conflict resolution skills
•Strong verbal and written communication skills
•Excellent documentation practices
•Attentive to detail, good initiative and able to work with changing priorities
•Computer skills an asset
•Ontario Society of Medical Technologist (OSMT) or equivalent certification an asset
•Knowledge of universal precautions
•2 – 3 years experience in phlebotomy and performing diagnostic 12 lead ECGs
•Previous experience in a CRO or pharmaceutical research environment is an asset
•Working knowledge of GCP, ICH, FDA and TPD regulations