Senior Project Manager, Oncology

Role overview Lead clinical research studies from planning through delivery, balancing quality, scope, budget, and timelines. Serve as the main client contact while coordinating cross-functional teams and external vendors on complex, often global trials.

Responsibilities - Build and maintain integrated study plans, timelines, budgets, forecasts, and risk mitigation actions. - Coordinate clinical operations, functional teams, and vendors; take on clinical activities when a study’s limited scope requires it. - Track study progress and finances, including profitability, billable hours, accurate invoicing, and out-of-scope work. - Maintain quality oversight, including inspection readiness and follow-up on quality findings or corrective actions. - Lead client and internal meetings, report performance and risks, and present issues and proposed responses to stakeholders. - Coordinate study-specific training and contribute to team feedback, performance reviews, and business development activities.

Requirements - Degree or equivalent experience in a science or health-related field; an advanced degree is preferred. - At least 7 years of clinical research experience and 4 years in direct project management, or demonstrated equivalent competencies. - Experience managing complex, global trials and working across functions. - Working knowledge of ICH-GCP, project planning, risk and change management, and escalation practices. - Experience with Microsoft Office, Microsoft Project, and clinical systems such as eTMF, EDC, and CTMS. - Strong communication, organization, attention to detail, and client service skills; able to travel domestically and internationally, including overnight.

Benefits and work setup The role includes eligibility for an annual discretionary bonus, health coverage, retirement savings, life and disability insurance, parental leave, and paid sick and vacation time. Candidates must already be authorized to work in the country of employment without sponsorship.