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Clinical Trials Part Time Jobs in Quebec (NOW HIRING)

Mcgill

Research Technician

Montreal, QC · On-site

CA$33.05 - CA$40.97/hr

... clinical trials in humans. This position involves collaborating with internal and external ... This position is a part-time, 3-month replacement contract. Major Duties and Responsibilities:

Mcgill

Research Technician

Montreal, QC · On-site

CA$33.05 - CA$40.97/hr

... clinical trials in humans. This position involves collaborating with internal and external ... This position is a part-time, 3-month replacement contract. Major Duties and Responsibilities:

Bayshore HealthCare

Registered Nurse

Montreal, QC

This is a part-time position with a commitment of 15 hours per week." RESUME DU POSTE L'Infirmier ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...

All JobsClinical Trials JobsClinical Trials Part Time JobsClinical Trials Part Time Jobs in Quebec

Clinical Trials Part Time information

What are the key skills and qualifications needed to thrive in a part-time clinical trials role, and why are they important?

To thrive in a part-time clinical trials role, you typically need a background in life sciences or healthcare, attention to detail, and familiarity with clinical research protocols. Experience with electronic data capture (EDC) systems, knowledge of Good Clinical Practice (GCP), and sometimes certification such as SOCRA or ACRP are commonly required. Strong organizational skills, clear communication, and adaptability help you excel in coordinating studies and working with diverse teams. These skills ensure accurate data collection, regulatory compliance, and efficient support of clinical research objectives.

What is a clinical trials part time job?

Clinical trials part time jobs are positions in which individuals assist with the planning, execution, or management of clinical research studies on a part-time basis. These roles may include research assistants, coordinators, data managers, or nurses, and offer flexible work hours to accommodate other commitments. Part-time staff are crucial in supporting the collection and management of data, participant recruitment, and ensuring compliance with study protocols. These positions are ideal for students, professionals seeking flexible hours, or those looking to gain experience in clinical research without committing to a full-time schedule.

What are the common responsibilities and challenges of working part-time in clinical trials?

Part-time roles in clinical trials typically involve supporting research coordinators, assisting with data collection and entry, participant recruitment, and ensuring compliance with study protocols. A common challenge can be balancing workload and communication with the team, as studies often require careful coordination and timely updates. Flexibility and strong organizational skills are important, as part-time staff may need to quickly adapt to changing priorities while maintaining high-quality standards. Despite these challenges, part-time positions offer valuable exposure to clinical research processes and can serve as a stepping stone to full-time roles or advanced positions in the field.

What is the difference between Clinical Trials Part Time vs Clinical Research Coordinator?

AspectClinical Trials Part TimeClinical Research Coordinator
CredentialsTypically requires a degree in health sciences or related field; certifications like CCRP are a plusRequires a degree in health sciences or related field; often holds certifications such as CCRP or CCRC
Work EnvironmentPart-time roles in clinics, hospitals, or research facilities; flexible schedulesFull-time or part-time roles in research sites, hospitals, or pharmaceutical companies
Employer & IndustryPharmaceutical companies, CROs, academic institutionsResearch sites, hospitals, pharmaceutical companies

Clinical Trials Part Time roles focus on supporting specific trial activities with flexible hours, while Clinical Research Coordinators oversee entire study processes, often working full-time. Both roles require similar credentials and are integral to clinical research, but differ mainly in scope and schedule.

What are the most commonly searched types of Clinical Trials jobs in Quebec? The most popular types of Clinical Trials jobs in Quebec are:
Clinical Trials Part Time jobs near you
Infographic showing various Clinical Trials Part Time job openings in Quebec as of August 2026, with employment types broken down into 2% As Needed, 76% Full Time, 15% Part Time, and 7% Contract. Highlights an 92% Physical, 2% Hybrid, and 6% Remote job distribution.

Research Technician

Mcgill

Montreal, QC • On-site

CA$33.05 - CA$40.97/hr

Part-time

Medical, Dental, Life, Retirement, PTO

Posted 16 days ago

Job description

Please refer to theHow to Apply for a Job (for External Candidates)job aid for instructions on how to apply.

If you are an active McGill employee (ie: currently in an active contract or position at McGill University), do not apply through this Career Site. Login to your McGill Workday account and apply to this posting using the Find Jobs report (type Find Jobs in the search bar).

Position Summary:

The Clinical Research Unit (CRU) of the Montreal Neurological Institute-Hospital (The Neuro) conducts over 100 clinical trials for patients with neurological disorders. The CRU is looking to hire a Research Technician to process, store, package and ship a wide variety of biological samples in the context of clinical trials in humans. This position involves collaborating with internal and external stakeholders including research coordinators, nurses and pharmaceutical companies. This position is a part-time, 3-month replacement contract.
Major Duties and Responsibilities:

  • Works closely with the Lab manager and Nurse manager to meet team objectives and ensure best practice in biological samples handling.
  • Ensure continuous support to research coordinators and nurses in the delivery of uptodate specialized technical laboratory tasks.
  • Performs a variety of tests including pregnancy tests; chemistry strip tests: pH, sediment levels, blood levels, leucocytes, proteins.
  • Records results, performs calculations, and compiles data.
  • Maintains individual study records for shipments.
  • Maintains inventory logs for each study kit, which includes: the quantity, the expiration date, and the location of the kit.
  • Participates actively in the review of laboratory processes and documentation for quality assurance and improvement as well as for audit preparedness.
  • Operates a variety of equipment, including centrifuge, incubator and temperature loggers.
  • Prepares and balances centrifuges, calibrates pipettes, ensures consumables are not expired, and manages temperature logs for the -80C and -20C freezers.
  • Arranges for examining and calibrating all laboratory equipment when applicable.
  • Read and understand clinical trial protocols and lab manuals related to each study.
  • Ensure that the activities are performed in accordance with clinical trial protocol and University and sponsor policies and procedures.
  • Always have an up-to-date certification for Good Clinical Practice (GCP), CRU Standard Operating Procedures (SOP), Health Canada Division 5, and IATA certification.
  • Maintains lab equipment and material inventory and communicates with coordinators/nurses the whereabouts of patient visit related lab equipment.
  • Responsible of maintaining a safe and unsoiled work environment.
  • Prepares chemical solutions required for testing and ensures they are appropriately combined with biological samples.
  • Conduct routine laboratory tests and analysis of samples.
  • Prepare, label, and sort blood, tissue and other samples from patients.

This job description is not an extensive and complete list of tasks related to the Research Technician role within the CRU.


Other Qualifying Skills and/or Abilities:

  • Undergraduate Degree (Biology or Sciences).
  • Prior experience handling biological samples (blood, saliva, urine, feces, cerebrospinal fluid, biopsy tissues).
  • Experience in clinical research and neuroscience.
  • Knowledge of IATA practices and biological sample processing.

Schedule

  • Part-time position, 25 hours/week.
  • Main hours of operations are regular business hours Monday to Friday with occasional evening and/or night shifts to accommodate long and overnight patient visits.

As one of Montreal's Top Employers, here is what we offer:

  • Competitive benefits package (Health, Dental, Life Insurance) (if eligible)

  • Defined contribution pension plan (with employer contribution up to 10%) (if eligible)

  • Group Registered Retirement Savings Plan (RRSP) and Tax Free Savings Account (TFSA)

  • Competitive vacation policy

  • Two (2) personal days

  • Two (2) floating holidays

  • Nine (9) "Summer Fridays" - paid days off between the St-Jean Baptiste holiday and Labour Day

  • Paid time off over the December holiday period

  • Tuition waiver for regular employees and their dependents

  • Up to two (2) days of remote work per week where the position permits


Before applying, please note that to work at McGill University, you must be both authorized to work in Canada and willing to work in the province of Quebec at the campus where the position is based / located.
Knowledge of English: McGill University is an English-language university where day to day duties may require English communication both verbally and in writing. The level of English required for this position has been assessed at a level 4 on a scale of 0-4.
For a definition of our language proficiency levels, please click here.

Minimum Education and Experience:

Bachelor's Degree - Biology 2 Years Related Experience /

Hourly Salary:

(MUNACA Level H) $33.05 - $40.97

Hours per Week:

25 (Part time)

Supervisor:

Manager, Operations

Position End Date (If applicable):

2026-11-09

Deadline to Apply:

2026-08-07

McGill University hires on the basis of merit and is strongly committed to equity and diversity within its community. We welcome applications from racialized persons/visible minorities, women, Indigenous persons, persons with disabilities, ethnic minorities, and persons of minority sexual orientations and gender identities, as well as from all qualified candidates with the skills and knowledge to productively engage with diverse communities. McGill implements an employment equity program and encourages members of designated groups to self-identify. Persons with disabilities who anticipate needing accommodations for any part of the application process may contact, in confidence, accessibilityrequest.hr@mcgill.ca.

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