Senior Project Manager - Oncology
New
J
JobgetherOncology clinical research
Based in CanadaFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- Professional fluency in English, both written and verbal, as well as fluency in the applicable local office language.
- Experience
- At least 7 years of clinical pharmaceutical industry experience, including demonstrated clinical project management capabilities; alternatively, more than 5 years of healthcare supervisory experience combined with 6 years of clinical research experience in the pharmaceutical or CRO industries.
- Required Skills
- NegotiationRisk Management
Requirements
- Hold a university or college degree, preferably in life sciences, or certification in a related allied health profession such as nursing, medical technology, or laboratory technology; equivalent education and experience may be considered.
- Have at least 7 years of clinical pharmaceutical industry experience, including clinical project management capabilities; alternatively, have more than 5 years of healthcare supervisory experience combined with 6 years of clinical research experience in the pharmaceutical or CRO industries.
- Have experience managing or leading multidisciplinary project teams and a thorough understanding of project management processes and project management software.
- Demonstrate financial acumen, including experience developing and managing project budgets, and have negotiation and commercial skills.
- Have thorough knowledge of ICH Guidelines, Good Clinical Practice (GCP), international regulatory requirements, and the drug development process.
- Have leadership, communication, organization, prioritization, and relationship-building skills.
- Be able to work independently and collaborate with colleagues and stakeholders across different cultures and time zones.
- Have professional fluency in English, written and verbal, and fluency in the applicable local office language.
- Be willing and able to travel domestically and internationally, including overnight stays, and have a valid passport and driver's license.
Responsibilities
- Lead cross-functional project teams and coordinate internal stakeholders, clients, vendors, and subcontractors across assigned clinical trials.
- Manage Phase I–IV clinical studies from start-up through close-out, overseeing scope, timelines, quality, budget, and delivery.
- Develop and maintain project plans, resource strategies, and contingency plans.
- Oversee project budgets and financial performance against established targets.
- Partner with functional leads to assess project issues, evaluate information, make business decisions, and implement solutions.
- Serve as a key client contact and ensure expectations are understood and addressed.
- Resolve project and team challenges through negotiation, prioritization, communication, and conflict management.
- Identify opportunities to improve project delivery efficiency and quality while ensuring compliance with clinical research standards and SOPs.
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