Senior Project Manager - Oncology

Accountabilities • Lead core and extended cross-functional project teams, coordinating internal stakeholders, clients, vendors, and subcontractors across assigned clinical trials.

• Manage Phase I–IV clinical studies from start-up through close-out, maintaining accountability for scope, timelines, quality, budget, and delivery.

• Develop and maintain comprehensive project plans, resource strategies, and contingency plans to support successful study execution.

• Oversee project budgets and financial performance, ensuring alignment with established targets.

• Partner with functional leads to assess complex project issues, evaluate information, make informed business decisions, and implement effective solutions.

• Serve as a key client contact, maintaining clear communication and ensuring 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 established SOPs.

Requirements:

• 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 also be considered.

• 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.

• Proven experience managing or leading multidisciplinary project teams, with a thorough understanding of project management processes and project management software.

• Strong financial acumen, including experience developing and managing project budgets, alongside effective negotiation and commercial skills.

• Thorough knowledge of ICH Guidelines, Good Clinical Practice (GCP), international regulatory requirements, and the drug development process.

• Excellent leadership, communication, organization, prioritization, and relationship-building skills.

• Ability to work independently and collaborate effectively with colleagues and stakeholders across different cultures and time zones.

• Professional fluency in English, both written and verbal, as well as fluency in the applicable local office language.

• Willingness and ability to travel domestically and internationally, including overnight stays, with a valid passport and driver's license.

Benefits:

• Remote work arrangement.

• Competitive compensation and a benefits package that varies depending on location.

• Salary information and compensation details discussed during the interview process.

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