Clinical Project Manager, Home-Based

    Toronto, ON, Canada
    • 5+ years clinical project management experience
    • Experience in oncology and/or CNS is required
    • Experience in P1, 2 and/or 3b trials

    Kelly Scientific Resources believes in relationships, not transactions. That’s why we’re committed to successfully matching job seekers with the best employers across Canada and around the world.  We fill positions from entry level to senior management, on a temporary or permanent basis. Whether your specialty is Science, Engineering, IT, Finance, Marketing, Manufacturing, Contact Centre or Business Administration, we’ll work with you to understand your likes, dislikes, goals and ambitions, and present you with opportunities that meet your needs. See what we have to offer.

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    • Build positive and productive relationships with sponsor, sites and other vendors
    • Develop a strong, high-communicating, high-performing, quality and relationship focused team
    • Clearly communicate goals, delegation of responsibility, performance expectations and feedback expectations
    • Track and proactively manage study metrics and timelines
    • Provide study projections
    • Proactively manage personnel resourcing needs
    • Track and review time and materials from a budget perspective monthly.  Coordinate with Managing Director of Operations and/or Clinical Operations Manager to ensure documentation secured for any out of scope activities prior to the activities taking place
    • Assess, analyze and proactively develop corrective action plans for investigational sites, vendors, sponsor and administrative issues
    • Ensure all team members are trained and oriented to the study
    • Ensure any additional training during the study is completed by the study team
    • Educate team on lessons learned (e.g. from audits, actions at sites etc.)
    • Attend internal Project Management meetings (L10 calls) and provide study updates, and scorecard metrics
    • SOP Mapping with the sponsor

    Education & Experience:

    • Degree in healthcare, sciencies, or related
    • 5+ years clinical project management experience
    • Experience in oncology and/or CNS is required
    • Experience in Phase 1, 2, and/or 3b trials
    • Strong relationship management
    • Integrity and Commitment
    • Enthusiasm (can-do attitude)
    • Strong computer skills (e.g. MS Word, Excel, SharePoint, Outlook)
    • Strong working knowledge of ICH/GCP Guidelines
    • Knowledge of drug development process
    • Strong leadership qualities; ability to challenge, inspire, enable, and encourage others




    Category: Clinical

    Reference ID: CA7677BM001539

    Date Posted: 25/06/2020


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