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Clinical Project Assistant Jobs in Quebec (NOW HIRING)

Alimentiv

Clinical Data Analyst

Quebec, QC · Remote

While evaluating new projects or requests for enhancements, help determine the project cost ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Alimentiv

Clinical Data Analyst

Montreal, QC · Remote

While evaluating new projects or requests for enhancements, help determine the project cost ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Alimentiv

Clinical Data Analyst

Sherbrooke, QC · Remote

While evaluating new projects or requests for enhancements, help determine the project cost ... These tools assist our recruitment team but do not replace human judgment. Final hiring decisions ...

Wealthy Recruiting

CA$50K - CA$60K/yr

... clinical solutions to healthcare providers across the country. For decades, we have partnered with ... projects moving forward. You will become an essential extension of the executive team, helping ...

RAVENSWOOD FAMILY HEALTH CENTER

$24 - $32/hr

POSITION SUMMARY Under direct supervision, the Medical Assistant provides clinical support in the ... Projects a professional image at all times, including adherence to dress code and standards of ...

Cree Board of Health and Social Services of James Bay (CBHSSJB)

The Nursing Unit includes the emergency/clinic department, medicine unit, hemodialysis unit, ambulatory clinic pilot project, and the social services department. The Clinical Unit includes the ...

New

Alimentiv

Medical Writer

Montreal, QC · On-site

... projects. Perform document quality control review when requested. Assist with writing or review of relevant training materials or work instructions as needed. Clinical Research/Academic Writing ...

Alimentiv

Statistician

Quebec, QC · Remote

Responsible for the application of biostatistical methods to support clinical trials and data ... Act as subject matter expert, providing statistical support to project teams, quality/study ...

Alimentiv

Statistician

Sherbrooke, QC · Remote

Responsible for the application of biostatistical methods to support clinical trials and data ... Act as subject matter expert, providing statistical support to project teams, quality/study ...

Alimentiv

Statistician

Montreal, QC · Remote

Responsible for the application of biostatistical methods to support clinical trials and data ... Act as subject matter expert, providing statistical support to project teams, quality/study ...

Altasciences

Scientist, Pk & Biomarker

Laval, QC · On-site

At Altasciences we all move in unison to assist and work in the discovery, development, and ... About The Role The Scientist, PK & Biomarkers is assigned to projects based on scientific ...

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All JobsClinical Project JobsClinical Project Assistant JobsClinical Project Assistant Jobs in Quebec

Clinical Project Assistant information

What is a clinical project assistant?

Clinical Project Assistants are support professionals who help manage and coordinate activities within clinical research projects. They assist project managers and clinical teams by handling administrative tasks, organizing documentation, scheduling meetings, and ensuring regulatory compliance. Their role is essential for keeping clinical trials running smoothly, maintaining accurate records, and facilitating communication among team members. Clinical Project Assistants often work in pharmaceutical companies, contract research organizations, or healthcare settings.

What are the key skills and qualifications needed to thrive as a clinical project assistant?

To thrive as a Clinical Project Assistant, you need strong organizational skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC), and regulatory documentation processes is typically required. Excellent communication, teamwork, and time management skills help you coordinate effectively with diverse stakeholders. These competencies are crucial for maintaining accurate trial documentation, ensuring regulatory compliance, and supporting efficient clinical study operations.

What are some common challenges faced by clinical project assistants, and how can they be managed effectively?

Clinical Project Assistants often encounter challenges such as managing multiple tasks across different projects, maintaining accurate and timely documentation, and ensuring effective communication among cross-functional teams. To manage these effectively, it's important to develop strong organizational and prioritization skills, utilize project management tools, and regularly communicate with project managers and team members to stay aligned on timelines and expectations. Proactive problem-solving and attention to detail can also help prevent issues and contribute to the smooth progress of clinical trials.

What is the difference between Clinical Project Assistant vs Clinical Research Coordinator?

AspectClinical Project AssistantClinical Research Coordinator
CredentialsTypically requires a bachelor's degree in health sciences or related fieldUsually requires a bachelor's degree; some roles prefer certification or experience
Work EnvironmentSupports project teams in clinical trial settings, often within pharmaceutical or biotech companiesManages and oversees clinical trials at research sites or hospitals
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, academic research centers, clinical trial sites
Search & Comparison IntentHigh overlap in job duties and required skills, often searched together

The Clinical Project Assistant primarily supports clinical trial projects by assisting with documentation, scheduling, and communication within the project team. In contrast, the Clinical Research Coordinator manages the day-to-day operations of clinical trials at research sites, including patient recruitment and data collection. While both roles require similar educational backgrounds and work in related environments, their responsibilities differ in scope and focus.

What are the most commonly searched types of Clinical Project jobs in Quebec?

The most popular types of Clinical Project jobs in Quebec are:

What cities in Quebec are hiring for Clinical Project Assistant jobs?

Cities in Quebec with the most Clinical Project Assistant job openings:

Clinical Project Assistant jobs near you
Infographic showing various Clinical Project Assistant 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 82% Physical, 2% Hybrid, and 16% Remote job distribution.

CRA 1/2 & Sr. CRAs - Oncology & General Medicine, French Speaking Desired- Canada

Montreal, QC • Remote

Fortrea
Health Care and Social Assistance • 10K+ employees

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

27th of 74 rated research

People enjoy working here

Good employer

Respectful managers

Learn more about Fortreaexternal

Full-time

Re-posted 14 days ago

Job description

We are currently seeking Experienced CRAs to lead and support our Full Service Outsourcing team supporting various sponsors. Oncology or Ophthalmology desired, seeking candidates on the East and West Coast of Canada. French Speaking candidates also desired. Will conduct 8-10 DOS per month, travel could be across Canada.

**CAR-T experienced Sr. CRAs located anywhere in Canada strongly desired!**

WHAT YOU WILL DO

You will utilize your skills, knowledge, and clinical judgement to provide a high standard of care for participants in clinical trials and respond to emergency situations based upon clinical research standards.

Responsibilities:

  • Responsible for all aspects of study site monitoring including routine monitoring and close-out of clinical sites, maintenance of study files, conduct of pre-study and initiation visits; liaise with vendors; and other duties, as assigned -
  • Responsible for all aspects of site management as prescribed in the project plans
  • General On-Site Monitoring
  • Ensure the study staff who will conduct the protocol have received the proper materials and instructions to safely enter patients into the study
  • Ensure the protection of study patients by verifying that informed consent procedures and protocol requirements are adhered to according to the applicable regulatory requirements
  • Ensure the integrity of the data submitted on Case Report Forms (CRFs) or other data collection tools by careful source document Monitor data for missing or implausible data
  • Responsible for all aspects of registry management as prescribed in the project plans - Undertake feasibility work when requested
  • Complete Serious Adverse Event (SAE) reporting, process production of repo11s, narratives and follow up of SAEs
  • Independently perform CRF review; query generation and resolution against established data review guidelines on Fortrea or client data management systems as assigned by management
  • Assist with training of new employees, eg. co-monitoring
  • Coordinate designated clinical projects as a Local Project Coordinator (with supervision, ifapplicable) and may act as a local client contact as assigned
  • Perform other duties as assigned by management

Requirements

  • University or college degree, or certification in a related allied health profession from an appropriately accredited institution (e.g. nursing licensure)
  • 1 - 3+ years of Clinical Monitoring experience
  • Oncology or ophthalmology experience is desired
  • Open to various hub locations in Canada
  • French Speaking preferred

The important thing for us is you are comfortable working in an environment that is:

  • Fast paced: where no deviations from the study protocol are allowed, and not meeting a timeline for even few minutes will create a quality issue.
  • Changing priorities constantly asking you to prioritize and adapt on the spot.
  • Teamwork and people skills are essential for the study to run smoothly.
  • Technology based. We collect our data directly into an electronic environment.

Work Environment:

  • Work is performed in an office environment with exposure to electrical office equipment.

  • Frequent travel to clients/ site locations with occasional travel both domestic and international.

Physical Requirements:

  • Ability to sit for extended periods and operate a vehicle safely.

  • Repetitive hand movement of both hands with the ability to make fast, simple, repeated movements of the fingers, hands, and wrists.

  • Occasional crouching, stooping, with frequent bending and twisting of upper body and neck.

  • Ability to access and use a variety of computer software developed both in-house and off-the-shelf.

  • Light to moderate lifting and carrying (or otherwise moves) objects including luggage and laptop computer with a maximum lift of 15-20 lbs.

  • Regular and consistent attendance.

  • Varied hours may be required.

#LI - Remote

Applications will be accepted on an ongoing basis.

Learn more about our EEO & Accommodations request here.

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