Clinical Program Manager

Adecco is currently hiring a Clinical Program Manager for our Medical Device Manufacturing client in Ottawa West. This is a permanent opportunity offering full time hours, Monday – Friday. The salary for this position will be determined based on education and experience. The client is also offering bonus and stock options.

Our client is a diversified health care innovator with a legacy of pioneering work in medical diagnostics and devices. They are dedicated to advancing innovative with-patient diagnostic technology to improve patient care and system efficiency by fundamentally changing the way health care professionals process patients through their system.

Position Overview: The Clinical Program Manager is responsible for strategy, management and execution of the clinical studies / projects for regulatory submission or evidence generation within program(s)

Responsibilities:

  • Determines applicable program or study objectives, strategy, scope and schedule to meet business needs.  Develops the project plan in consultation with the cross-functional program or project team, project stakeholders and the clinical team.  Presents project plans, provides ongoing updates and presents project results to Division senior clinical management.
  • Manages and oversees the execution of the clinical program or projects (multiple clinical studies).
  • Ensures staff are trained on the requirements of the clinical project and the project plan.
  • Manages and directs the clinical team members (clinical project managers, CRAs) working on the clinical program.
  • Motivates and develops staff.
  • Responsible for ensuring the clinical project is audit-ready at all times (e.g. project team training records, central files, system validation, etc.)
  • Ensures adequate monitoring is conducted on all clinical projects.
  • Conducts clinical visits to support clinical projects.
  • Provides oversight of clinical project to ensure safety concerns and/or adverse events or trends in Field Events Reporting are identified and appropriate responses are developed an executed.
  • Controls device distribution and allocation.
  • Monitors project reports for accuracy and trending.  Projects input to project budgets and project plans,
  • Provides clinical scientific support to project teams.
  • Evaluates clinical data in preparation of study summary reports for presentations, publications and submissions.
  • Develops and implements corrective actions as needed to address any noncompliance issues.
  • Communicates with, and provides updates to, specific core teams.
  • Other miscellaneous duties as may be required.
  •  

    Required Education and Experience:

  • Minimum of 7 years directly supporting clinical research or similar experience in a medical/scientific area
  • Minimum of 10 years managing projects and working with clinical professionals within a team as well as working in a cross-functional project development setting
  • High attention to detail and accuracy
  • Advanced written and oral communication skills
  • Able to manage multiple tasks and priorities
  • Proficient knowledge of medical terminology
  • Expertise with GCPs and regulatory compliance for clinical trials (e.g. applicable ISO Standards, FDA)Strong problem-solving skills
  • Bachelor’s degree in Engineering, Science or related field
  • Advanced degree (Masters or Phd) is an asset
  • To be considered for the Clinical Program Manager opportunity, please Apply Now!

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    • Apply with Adecco

    Reference number CA_EN_1_021956_1688770

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