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Remote Clinical Project Manager Jobs in Toronto, ON

CTLs partner with the Project Manager and other functional leads to ensure successful delivery of ... Standard Office Environment or remote based work required * Weekend and off-hour work as required

Project Manager (Remote)

Aurora, ON · Remote

CA$80K - CA$135K/yr

As a Project Manager , you will provide overall leadership and direction for assigned construction projects, ensuring successful delivery from project pursuit through to close-out. You will be ...

As a Project Manager within the Enterprise Applications Business Unit at Datavail you will provide ... Lead and direct a remote project team to be successful * This position will focus on delivery of ...

As a Project Manager within the Enterprise Applications Business Unit at Datavail you will provide ... Lead and direct a remote project team to be successful * This position will focus on delivery of ...

Developing and managing project-specific change and risk management systems * Ensuring project ... remote locations * Knowledge of applicable codes and standards. Knowledge of Russian design ...

This role is open to both candidates based in the United States who are able to work fully remote ... S. regulatory landscape, solid project management discipline, and the judgment and leadership ...

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Remote Clinical Project Manager information

What is a remote clinical project manager?

A Remote Clinical Project Manager is a professional who oversees clinical research projects from a remote location, rather than being based on-site. Their primary responsibilities include planning, executing, and managing clinical trials to ensure they are completed on time, within budget, and in compliance with regulatory standards. They coordinate with cross-functional teams, monitor study progress, and maintain communication with stakeholders. By working remotely, they utilize digital tools and platforms to manage tasks, meetings, and documentation efficiently.

How does a remote clinical project manager effectively coordinate with cross-functional teams spread across different locations?

As a Remote Clinical Project Manager, you'll regularly collaborate with cross-functional teams—including clinical research associates, data managers, regulatory specialists, and external vendors—often located in various regions or countries. Effective coordination is achieved through regular virtual meetings, clear documentation, and leveraging project management tools to track progress and share updates. Strong communication skills are essential to align timelines, address challenges proactively, and ensure all stakeholders are informed and engaged. Embracing digital collaboration platforms and fostering a transparent, supportive team culture are key to overcoming the complexities of remote, multi-site clinical trials.

What is the difference between Remote Clinical Project Manager vs Remote Clinical Research Associate?

AspectRemote Clinical Project ManagerRemote Clinical Research Associate
Required CredentialsTypically requires a Bachelor's degree in life sciences, project management certification (e.g., PMP), and experience in clinical trials.Usually requires a Bachelor's degree in life sciences or related field, with some roles preferring certification like CCRP.
Work EnvironmentManages multiple clinical trials, oversees teams, and coordinates with sponsors remotely.Monitors clinical sites, ensures protocol compliance, and collects data remotely.
Employer & Industry UsageCommonly employed by pharmaceutical companies, CROs, and biotech firms.Primarily employed by CROs, pharmaceutical companies, and research institutions.

The Remote Clinical Project Manager and Remote Clinical Research Associate roles share overlapping credentials and industry settings. However, the Project Manager oversees entire clinical projects and teams, while the Research Associate focuses on site monitoring and data collection. Both roles are essential in clinical research and often work remotely within the same industry sectors.

What are the key skills and qualifications needed to thrive as a remote clinical project manager, and why are they important?

To thrive as a Remote Clinical Project Manager, strong project management abilities, clinical research knowledge, and a relevant degree in life sciences or healthcare are essential. Familiarity with tools like Microsoft Project, electronic data capture (EDC) systems, and certifications such as PMP or ACRP/SoCRA are typically required. Exceptional communication, leadership, and problem-solving skills help coordinate remote teams and stakeholders effectively. These skills ensure successful clinical trial execution, regulatory compliance, and timely delivery of project milestones in a virtual environment.
What are popular job titles related to Remote Clinical Project Manager jobs in Toronto, ON? For Remote Clinical Project Manager jobs in Toronto, ON, the most frequently searched job titles are:
Infographic showing various Remote Clinical Project Manager job openings in Toronto, ON as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution.

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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