Research Assistant 1
Montreal, QC · On-site
CA$30.54/hr
... Assistant 2). Assist with the recruitment, consent, and follow-up of participants with ... relevant clinical trials. (iv) Contact participants outside of clinic, including first-degree ...
Montreal, QC · On-site
CA$30.54/hr
... Assistant 2). Assist with the recruitment, consent, and follow-up of participants with ... relevant clinical trials. (iv) Contact participants outside of clinic, including first-degree ...
Montreal, QC · On-site
CA$30.54/hr
... Assistant 2). Assist with the recruitment, consent, and follow-up of participants with ... relevant clinical trials. (iv) Contact participants outside of clinic, including first-degree ...
Montreal, QC · On-site
CA$30.54/hr
... Assistant 2). Assist with the recruitment, consent, and follow-up of participants with ... relevant clinical trials. (iv) Contact participants outside of clinic, including first-degree ...
Montreal, QC · On-site
CA$30.54/hr
... Assistant 2). Assist with the recruitment, consent, and follow-up of participants with ... relevant clinical trials. (iv) Contact participants outside of clinic, including first-degree ...
Montreal, QC · On-site
... the Clinical Trial Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in preparing draft budgets and cost justifications for industry-sponsored trials.
Montreal, QC · On-site
... the Clinical Trial Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in preparing draft budgets and cost justifications for industry-sponsored trials.
Montreal, QC · On-site
... the Clinical Trial Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in preparing draft budgets and cost justifications for industry-sponsored trials.
Montreal, QC · On-site
... the Clinical Trial Management System (CTMS). Primary Responsibilities: Administrative and Budget Support * Assist in preparing draft budgets and cost justifications for industry-sponsored trials.
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... * Assist with training of new employees, eg. co-monitoring * Coordinate designated clinical ...
Montreal, QC · Remote
... clinical trials and respond to emergency situations based upon clinical research standards ... * Assist with training of new employees, eg. co-monitoring * Coordinate designated clinical ...
Montreal, QC · On-site
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
Montreal, QC · On-site
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
$180 - $240/hr
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
$180 - $240/hr
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
Montreal, QC · On-site
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
Montreal, QC · On-site
Review Serious Adverse Events, SUSARs, safety narratives and perform Analysis of Similar Events * Assist clinical data management with MedDRA and WHO coding in assigned trials * Assist by reviewing ...
Quebec, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
Quebec, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
Sherbrooke, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
Sherbrooke, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
Montreal, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
Montreal, QC · Remote
Responsible for the application of biostatistical methods to support clinical trials and data ... Study Report Support * Assist medical director(s) and/or technical writers by preparing statistical ...
... trials. The Sample Management Coordinator will ensure tasks performed are conducted within ... Act as a liaison to the clinical/study operations teams. * Assist in the resolution of data queries.
New
... trials. The Sample Management Coordinator will ensure tasks performed are conducted within ... Act as a liaison to the clinical/study operations teams. * Assist in the resolution of data queries.
New
At Altasciences we all move in unison to assist and work in the discovery, development, and ... use during clinical trials. * Assign equipment asset tags to newly inventoried equipment.
At Altasciences we all move in unison to assist and work in the discovery, development, and ... use during clinical trials. * Assign equipment asset tags to newly inventoried equipment.
... requirements * Assist management in monitoring sales pricing practices to ensure accuracy and ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
Quick apply
... requirements * Assist management in monitoring sales pricing practices to ensure accuracy and ... stage clinical trials. The Company operates globally with facilities located in Canada, USA ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
... assister a des conferences et de participer a des essais cliniques. Bayshore met l'accent sur la ... clinical trials. Bayshore has a focus on nursing education and provides many opportunities for ...
$12.74 - $14.90
15% of jobs
$15.65 is the 25th percentile. Wages below this are outliers.
$14.90 - $17.07
30% of jobs
The median wage is $18.15 / hr.
$17.07 - $19.23
10% of jobs
$19.23 - $21.39
19% of jobs
$21.94 is the 75th percentile. Wages above this are outliers.
$21.39 - $23.56
4% of jobs
$23.56 - $25.72
8% of jobs
$25.72 - $27.88
6% of jobs
$27.88 - $30.05
2% of jobs
$30.05 - $32.21
0% of jobs
$32.21 - $34.38
0% of jobs
$34.38 - $36.54
5% of jobs
$12
$20
$36
| Aspect | Clinical Trials Assistant | Clinical Research Coordinator |
|---|---|---|
| Credentials | High school diploma or equivalent; some roles may require certification | Bachelor’s degree in health sciences or related field; often requires certification |
| Work Environment | Research sites, hospitals, clinics, pharmaceutical companies | Research sites, hospitals, clinics, pharmaceutical companies |
| Responsibilities | Assist with data entry, document management, and trial logistics | Oversee trial processes, patient recruitment, data collection, and compliance |
| Industry Usage | Commonly used in clinical trial support roles | More involved in trial management and coordination |
While both roles support clinical trials, Clinical Trials Assistants focus on administrative and logistical tasks, whereas Clinical Research Coordinators handle more comprehensive trial management, patient interactions, and compliance activities.
The most popular types of Clinical Trials jobs in Quebec are:
For Clinical Trials Assistant jobs in Quebec, the most frequently searched job titles are:
The top searched job categories for Clinical Trials Assistant jobs in Quebec are:
Cities in Quebec with the most Clinical Trials Assistant job openings:

CA$30.54/hr
Full-time
This job post has expired today. Applications are no longer accepted.
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Provide operational support to the Neuroimmunology clinical research program, under the supervision of the investigators (Harroud A., Thebault S., Blanchard O., and Giacomini P.) and senior research staff (Research Assistant 2). Assist with the recruitment, consent, and follow-up of participants with neuroimmunological diseases, including but not limited to multiple sclerosis, neuromyelitis optica spectrum disorder, MOG antibody-associated disease, and myasthenia gravis. Support the collection and documentation of clinical information and biological samples, and ensure that activities are carried out in accordance with established research protocols, ethical approvals, and institutional procedures. Act as a liaison between patients, clinical staff, and the investigators to facilitate ongoing observational and biomarker studies.
TYPICAL FUNCTIONS:
(i) Attend relevant outpatient clinics (e.g. MS clinic, lumbar puncture clinic) to approach, inform, and consent eligible participants to research studies, in coordination with clinical staff. Document consent in the appropriate systems and ensure proper creation, storage, and filing of study identifiers and forms.
(ii) Coordinate the collection of biological samples (e.g. blood, CSF, DNA) from enrolled participants, including arranging collection during visits, ensuring linkage between samples and participant records, and supporting related logistics (scheduling, transport, documentation).
(iii) Conduct pre-visit review of scheduled patients to identify those already enrolled in studies, those requiring biospecimen collection, and those prioritized for specific projects (e.g. treatment-naive patients, neuromyelitis optica spectrum disorder, MOG antibody-associated disease, myasthenia gravis). Contribute to improving screening and tracking workflows, including identifying candidates for imaging studies and relevant clinical trials.
(iv) Contact participants outside of clinic, including first-degree relatives of patients and referred patients from external centres, to explain studies, confirm eligibility, obtain or document consent, administer or monitor questionnaire completion (e.g. REDCap), and coordinate biospecimen collection.
(v) Work jointly with the Clinical Research Unit (CRU) to identify and refer eligible patients for clinical trials. Collaborate with investigators involved in MRI-based research to identify and refer interested participants for imaging studies.
(vi) Maintain accurate, confidential, and up-to-date records of recruitment activity, communication with participants, biospecimen collection, and imaging/trial referrals; flag issues to investigators.
(vii) Perform other related duties in support of the Neuroimmunology research program, as required.
EDUCATION AND EXPERIENCE:
- Bachelor's degree in a relevant field (e.g. neuroscience, biology, biomedical science) or equivalent training and experience.
- Experience in a clinical or research setting involving direct interaction with patients is an asset.
- Experience with clinical research or human biospecimen handling is an asset.
Other Qualifying Skills and/or Abilities:
Demonstrated ability to interact professionally and empathetically with patients and families. Strong organization and attention to detail, with the ability to manage several activities in parallel. Capable of interpreting, implementing, and enforcing research protocols, regulatory requirements, and ethical standards. Ability and willingness to perform, or be trained to perform, phlebotomy/venipuncture and to handle biospecimens; experience with basic wet lab techniques for sample processing is an asset. Ability with databases and electronic data capture tools (e.g. REDCap, spreadsheets) is required; coding experience is an asset. Full professional proficiency in English and French is required.
Hiring unit: MNI
This position is covered by the AMURE collective agreement: http://www.aerum-amure.ca/wp-content/uploads/2023/07/AMURE-2023-2027.pdf
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.
McGill University is an English-language university where most teaching and research activities are conducted in the English language, thereby requiring 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.
Hourly Salary:
Hours per Week:
Location:
Supervisor:
Position Start Date:
Position End Date:
Deadline to Apply:
This position is covered by the Association ofMcGill University Research Employees(AMURE) collective agreement.
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.