Senior Project Manager - Oncology
New
Fully remote work flexibility within Canada.Full-TimeSenior
Salary163,800 - 245,800 CAD per year
Apply NowOpens the employer's application page
Job Details
- Experience
- Minimum of 7 years of clinical research experience, including at least 4 years in direct project management roles.
- Required Skills
- Project ManagementQuality AssuranceRisk Management
Requirements
- Bachelor’s degree in a science or health-related field or equivalent professional experience; advanced degree preferred.
- Minimum of 7 years of clinical research experience, including at least 4 years in direct project management roles.
- Strong experience managing complex, global clinical trials within pharmaceutical, biotechnology, medical device, or CRO environments.
- Proven expertise in oncology clinical research; experience with cell and gene therapy is highly preferred.
- Deep understanding of ICH-GCP guidelines, clinical operations, risk management, and quality assurance practices.
- Experience with project management and clinical research systems such as CTMS, EDC, eTMF, Microsoft Project, and Microsoft Office Suite.
- Strong leadership, organizational, communication, negotiation, and stakeholder management skills.
- Ability to manage budgets, timelines, operational risks, and cross-functional collaboration effectively.
- Demonstrated experience presenting to clients, leading meetings, and supporting bid defense activities.
- Willingness and ability to travel domestically and internationally as required.
- Results-oriented mindset with strong analytical, decision-making, and problem-solving capabilities.
Responsibilities
- Serve as the primary point of contact for clients, ensuring clear communication, relationship management, and issue escalation throughout clinical study execution.
- Lead and coordinate cross-functional teams, vendors, and operational stakeholders to deliver oncology clinical trials within established timelines, budgets, and quality standards.
- Develop and maintain comprehensive project plans, including risk management, mitigation strategies, and operational oversight across all study phases.
- Manage project financials, including profitability, forecasting, billing accuracy, and identification of out-of-scope activities.
- Oversee quality management activities, ensuring inspection readiness, compliance with regulatory standards, and implementation of corrective and preventive action plans when necessary.
- Monitor study progress through KPIs, tracking metrics, and regular reporting to clients and senior leadership.
- Lead internal and external project meetings, presentations, and bid defense activities with professionalism and strategic insight.
- Support study-specific training initiatives and ensure compliance with operational procedures and clinical research standards.
- Contribute to business development initiatives and collaborate on process improvement opportunities across clinical operations.
- Mentor and provide ongoing feedback to team members, fostering collaboration, accountability, and high performance.
View Full Description & ApplyYou'll be redirected to the employer's site
