Senior Project Manager

Canada-basedFull-TimeSenior
Salary not disclosed
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Job Details

Experience
Several years of experience in clinical project management
Required Skills
Project ManagementGCPRisk ManagementStakeholder managementBudget management

Requirements

  • Bachelor’s degree in Life Sciences, Healthcare, Pharmacy, or a related field; advanced degree preferred.
  • Several years of experience in clinical project management within a CRO, pharmaceutical, or clinical research environment.
  • Strong knowledge of clinical trial processes, GCP regulations, and regulatory compliance requirements.
  • Proven ability to manage complex, multi-site, global clinical studies with cross-functional teams.
  • Strong financial acumen with experience managing project budgets, forecasts, and profitability.
  • Excellent communication, leadership, and stakeholder management skills, including client-facing experience.
  • Ability to manage risk, resolve operational challenges, and maintain high attention to detail in a regulated environment.
  • Proficiency with clinical trial management systems and project tracking tools is an asset.

Responsibilities

  • Lead end-to-end project management of clinical research studies, ensuring delivery against scope, timelines, quality standards, and budget requirements.
  • Serve as the primary liaison between clients and internal teams, coordinating communication and ensuring alignment across all study phases.
  • Oversee cross-functional study teams and external partners, managing deliverables and proactively addressing risks, issues, and dependencies.
  • Ensure full compliance with GCP guidelines, SOPs, and applicable regulatory requirements throughout study execution.
  • Maintain oversight of financial performance, project forecasting, and budget control for assigned studies.
  • Drive development of project plans, risk mitigation strategies, and contingency planning to ensure operational success.
  • Prepare governance materials, client reports, and presentations, while ensuring study documentation and systems are inspection-ready.
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