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Associate Clinical Project Manager Jobs in Toronto, ON

CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical ...

Performs clinical supplies management with vendors on a country and regional level. * Ensures study ... Manages the project team in site contracting and payments. * Leads project team calls on a country ...

POSITION OVERVIEW The Associate Project Manager has the primary responsibility to coordinate the execution of all projects (TV, Digital, Print, Mobile, etc.) for all assigned brands. This position is ...

Project Manager

Toronto, ON · On-site

CA$86K/yr

... clinical medicine, basic science and the rehabilitation sciences sectors. Your opportunity: The ... As Project Manager, you will you will play an instrumental role in leading the planning ...

Directs, manages, and coordinates team members including other project managers, business and technology resources, user groups, internal and external consultants and contractors, as well as vendors ...

New

Must have project management or clinical equipment and furniture coordination experience in a redevelopment project within the last 5 years. * Must have experience in the selection, specification ...

Project Manager

Oakville, ON

CA$100K - CA$120K/yr

You, as a Project Manager, Facilities Services will: * Have oversight from pre-construction to ... Meet with Hospital Clients, end users and other clinical teams, as well as Consultants and ...

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Associate Clinical Project Manager information

See Toronto, ON salary details

$12

$41

$75

How much do associate clinical project manager jobs pay per hour?

As of Aug 4, 2026, the average hourly pay for associate clinical project manager in Toronto, ON is $41.47, according to ZipRecruiter salary data. Most workers in this role earn between $27.53 and $53.68 per hour, depending on experience, location, and employer.

What is an associate clinical project manager?

An Associate Clinical Project Manager (ACPM) is an entry- to mid-level professional who assists in planning, coordinating, and overseeing clinical trials and research projects within pharmaceutical, biotech, or clinical research organizations. They work closely with project managers and cross-functional teams to ensure studies are conducted according to protocol, regulatory requirements, and timelines. ACPMs may handle tasks such as tracking project progress, supporting site management, preparing documentation, and communicating with stakeholders. Their role helps ensure the smooth execution and delivery of clinical research projects.

What are the common challenges faced by an associate clinical project manager and how can they be addressed?

Associate Clinical Project Managers often encounter challenges such as balancing multiple study timelines, coordinating cross-functional teams, and ensuring regulatory compliance. Managing communication between sponsors, vendors, and internal teams can also be complex. To address these challenges, it's important to prioritize tasks, maintain clear documentation, and foster strong relationships with stakeholders. Leveraging project management tools and regularly reviewing project milestones can help ensure studies stay on track and issues are promptly resolved.

What are the key skills and qualifications needed to thrive as an associate clinical project manager?

To thrive as an Associate Clinical Project Manager, you need a solid understanding of clinical research processes, project management principles, and typically a degree in life sciences or a related field. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Exceptional organizational skills, attention to detail, and strong communication abilities help you coordinate teams and timelines effectively. These competencies are crucial for ensuring clinical trials run smoothly, meet regulatory standards, and deliver reliable results on schedule.

What is the difference between Associate Clinical Project Manager vs Clinical Project Coordinator?

AspectAssociate Clinical Project ManagerClinical Project Coordinator
CredentialsBachelor's degree, often some project management or clinical research experienceBachelor's degree, entry-level in clinical research
Work EnvironmentSupports project managers, involved in planning and oversightAssists with daily tasks, data collection, and site communication
Employer & Industry UsagePharmaceutical, biotech, clinical research organizationsClinical research sites, CROs, pharma companies

The Associate Clinical Project Manager typically has more responsibility in project planning and oversight compared to the Clinical Project Coordinator, who mainly supports data collection and site coordination. Both roles are essential in clinical research teams, with the associate role often serving as a stepping stone to more senior project management positions.

What are the most commonly searched types of Clinical Project Manager jobs in Toronto, ON? The most popular types of Clinical Project Manager jobs in Toronto, ON are:
What are popular job titles related to Associate Clinical Project Manager jobs in Toronto, ON? For Associate Clinical Project Manager jobs in Toronto, ON, the most frequently searched job titles are:
Infographic showing various Associate Clinical Project Manager job openings in Toronto, ON as of July 2026, with employment types broken down into 1% As Needed, 72% Full Time, 25% Part Time, 1% Temporary, and 1% Contract. Highlights an 93% Physical, 4% Hybrid, and 3% Remote job distribution, with an average salary of $86,250 per year, or $41.5 per hour.

Clinical Team Lead, Phase I

Fortrea

Toronto, ON • Remote

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 11 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 72 rated research


Job description

We are currently seeking an experienced Clinical Trial Manager to join our Phase I team! Homebased within the US or Canada.

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.

Job Overview:

Clinical Team Leads (CTL) own the clinical delivery of clinical research trials. CTLs function as the Clinical Project Manager (CPM) within the core project team. CTLs partner with the Project Manager and other functional leads to ensure successful delivery of the clinical aspects of a trial within contractual and budgetary requirements. The CTL oversees the clinical and site management aspects of the trial. The CTL represents clinical delivery with the given customer.

    Responsibilities:

    • Take accountability for proactively driving clinical project performance toward contracted deliverables while meeting customer needs and maintaining operational excellence.
    • Drive communication and collaboration with the client and project team across a matrixed, multicultural, environment.
    • Lead the development of the clinical project strategy and ensures prioritization with the clinical project team and key stakeholders in the creation of clear, data driven strategies and proactive management of project scope, timelines, quality and budget. In collaboration with relevant departments, prepare and deliver presentations for new business as required.
    • Manage the operational aspects of projects to support subject recruitment and retention, clinical vendor delivery and oversee the monitoring visit strategy.
    • Identify clinical project, financial and quality risks leveraging end to end risk management practices and quality by design principles.
    • Appropriately utilize data sources, dashboards and risk management strategies to drive innovation and proactive problem solving with the project and client teams.
    • Adhere to project governance and issue escalation pathways, ensuring that clinical project plans are in place to address identified risk while adhering to professional standards, SOPs, client and regulatory requirements
    • Partner with project team members and key stakeholders to oversee and manage clinical project budgets, resources and scope.
    • Ensure adherence to established budget and financial milestones. Accountable for accurately forecasting clinical project revenue and managing project costs in adherence to the budget.
    • Leading the timely management of changes to scope and the change order process. Ensures project team awareness and tracking of KPIs for any client specific metrics.
    • Provide inspiring leadership and play a key role in the creation of high performing clinical project teams. Facilitating communication and teamwork while driving delivery, ensuring that clinical team members understand contracted scope, timelines and budget.
    • Ensures that clinical resource projections are accurate and visible to resourcing teams, proactively escalating resource constraints and challenges.
    • Develops and mentors team members in multiple areas of expertise and provide feedback as needed to respective line managers
    • As required by the project roles participate and oversee the regulatory/ethics committee submissions, tracking, and documentation.
    • Support new business with active participation in Bid Defense preparation and meetings, as required.
    • And all other duties as needed or assigned

    Qualifications (Minimum Required):

    • University/college degree (life science preferred) or certification in a related allied health profession (i.e. nursing, medical or laboratory technology) from an appropriately accredited institution
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.
    • Fluent in English, both written and verbal.

    Experience (Minimum Required):

    • 2+ years of Clinical Team Lead experience or an equivalent combination of education and experience to successfully perform key responsibilities of the job.
    • Working knowledge of ICH Guidelines and GCP including international regulatory requirements for the conduct of clinical development programs.
    • Advanced computer skills (e.g., Microsoft Word, Excel, Project, Access and Power Point).
    • Experience managing projects in a matrix and virtual environment.
    • Excellent communication, planning and organizational skills.
    • Demonstrated ability to lead by example and to encourage team members to seek solutions independently Demonstrated ability to handle multiple competing priorities and to utilize resources effectively.
    • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix system.
    • Financial awareness and ability to actively and effectively utilize financial tracking systems.
    • Ability to work independently and mentor junior project team members.
    • Ability to negotiate and liaise with clients in a professional manner.
    • Ability to present to staff at all levels.

    Preferred Qualifications Include:

    • Master or other advanced degree
    • PMP certification 2+ years CRA experience, on-site or in-house
    • Phase I/FIH experience
    • In lieu of the above minimum requirement, candidates with three or more years of relevance clinical research experience in pharmaceutical, CRO or health care setting will be considered

    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.

    What do you get?

    Regular, full-time or part-time employees working 20 or more hours per week are eligible for comprehensive benefits including but not limited to:

    • Medical, Dental, Vision, Life, STD/LTD (multiple insurance carriers)

    • 401(K)

    • Paid time off (PTO) - Flex Plan

    • Employee recognition awards

    • Multiple ERG's (employee resource groups)

    • Target Pay Range (based on title): $135-145K

    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 Demands/Work Environment:

    • Standard Office Environment or remote based work required
    • Weekend and off-hour work as required
    • Travel Requirements: up to 30% (Global - primary domestic and international)

    #LI - Remote

    Applications will be accepted on an ongoing basis.

    Learn more about our EEO & Accommodations request here.


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