ZipRecruiter

Log In

1

Clinical Project Assistant Jobs in Quebec (NOW HIRING)

Altasciences

Manager, Clinical Monitoring

Laval, QC · On-site

At Altasciences we all move in unison to assist and work in the discovery, development, and ... Serve as a management contact for sites, project teams, and sponsors when issues related to ...

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

Under the authority of the Assistant Director, Chisasibi Regional Hospital, the incumbent will plan ... and clinical priorities. SPECIFIC FUNCTIONS • Ensures that services are provided within the ...

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

Under the authority of the Assistant Director, Chisasibi Regional Hospital, the incumbent will plan ... and clinical priorities. SPECIFIC FUNCTIONS • Ensures that services are provided within the ...

Alimentiv

Consulting Statistician

Sherbrooke, QC · On-site +1

Creates supplementary materials such as slides or reports to assist in communication and ... Prepares statistical analysis plans and oversee project data collection, management, and analysis ...

Alimentiv

Consulting Statistician

Montreal, QC · On-site +1

Creates supplementary materials such as slides or reports to assist in communication and ... Prepares statistical analysis plans and oversee project data collection, management, and analysis ...

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 ...

Harris

Intern Developer

Quebec, QC

CA$20/hr

... assist in building and releasing products ... You will help develop ancillary parts of larger development projects and as skills progress have ...

Alimentiv

Business Development Director

Montreal, QC

Support the Clinical operations teams in identifying and sourcing new vendors required for projects following all Alimentiv and industry standard requirements. * Assist with the creation, review and ...

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 ...

next page

Showing results 1-20

All JobsClinical Project Assistant JobsClinical Project Assistant Jobs in Quebec

Clinical Project Assistant information

See Quebec salary details

$11

$33

$69

How much do clinical project assistant jobs pay per hour?

As of Jun 16, 2026, the average hourly pay for clinical project assistant in Quebec is $33.38, according to ZipRecruiter salary data. Most workers in this role earn between $21.39 and $37.50 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Clinical Project Assistant, and why are they important?

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 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 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 are Clinical Project Assistants?

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 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
Clinical Trials Associate - Canada - Remote

Clinical Trials Associate - Canada - Remote

Worldwide Clinical Trials

Quebec, QC • On-site

Full-time

Posted 7 days ago

Job description

Who we are

We're a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world's most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence.

We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs - in the best possible way.

Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit.

Why Worldwide

We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day.Join us!

What the Clinical Trial Associate does at Worldwide

As a Clinical Trials Associate, you are responsible for providing administrative and project tracking support to the clinical project team, ensuring tasks for all assigned projects with Project Delivery services are performed timely and accurately.

What you will do

  • Arrange and track system access for project team (Project Managers, Lead CRAs, CRAs, etc.)

  • Maintain and quality audit to assure the most recent revisions of documents are on project portals

  • Assist project team with preparation and shipment of clinical trial documentation, including Investigator Site File

  • Maintain version and quality control of project documentation and submit to trial master file

  • Assist with the tracking and maintenance of project related information, including site medical question and answer log

What you will bring to the role

  • Excellent written and verbal English as well as fluency of the language of the country of location

  • Ability to handle multiple tasks and exercise independent judgment

  • Strong attention to detail and focus on quality of work

  • Strong organizational and problem-solving skills

  • Excellent skills in MS Office applications including Outlook, Word, Excel and PowerPoint

Your experience

  • Degree level qualification or equivalent experience plus a minimum of one years' experience in a related role

  • Skill sets and proven performance equivalent to the above

We love knowing that someone is going to have a better life because of the work we do.

To view our other roles, check out our careers page at Discover a world of difference at Worldwide!For more information on Worldwide, visit www.Worldwide.com or connect with us on LinkedIn.

Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative,innovative,and successful. We'reon a mission to hire thevery bestand are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.

Apply