Senior Project Manager - Oncology; U.S

Join a global Contract Resource Organization (CRO) where innovation meets purpose. At Worldwide Clinical Trials
, we're driven by a shared commitment to improving lives through high-quality clinical research. Our teams are empowered to think creatively, take ownership, and deliver meaningful work that helps bring life-changing therapies to patients around the world.

With more than 4,000 professionals across the globe, we foster a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact. Whether you're building your career or bringing years of experience, you'll have the opportunity to learn, grow, and help shape the future of clinical research.

Take ownership of complex Phase I–IV clinical trials and lead them from start-up through close-out. As a Senior Project Manager at Worldwide, you’ll be accountable for bringing together the people, plans, and resources needed to deliver successful local, regional, or global studies.

You’ll combine clinical project leadership with financial and operational oversight, partnering with cross-functional teams to solve challenges, manage risk, and keep programs aligned with client expectations for time, quality, and cost.

As a key client contact, you’ll also build strong relationships with client teams and vendors while creating an environment where multidisciplinary project teams can perform at their best.

This is a remote role open to candidates based in United States. You will collaborate with global teams across multiple time zones. Ability to travel 10% is required.

• Lead core and extended cross-functional project teams, coordinating internal partners, clients, vendors, and subcontractors across assigned clinical trials.
• Manage Phase I–IV clinical trials from start-up through close-out, maintaining accountability for project scope, timelines, quality, cost, and delivery.
• Develop and maintain project plans, resource strategies, and contingency plans to support successful study execution.
• Drive financial performance by managing project budgets and working toward established financial targets.
• Partner with functional leads to evaluate complex project issues, interpret information, make sound business decisions, and implement effective solutions.
• Build strong client relationships as a key project contact, maintaining clear communication and helping ensure client expectations are met.
• Resolve project and team challenges through effective communication, negotiation, prioritization, and conflict management.
• Improve the efficiency and quality of project delivery while ensuring teams operate in accordance with established clinical research standards and SOPs.

• 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; an equivalent combination of education and experience that provides the required knowledge and capabilities will also be considered.
• At least 7 years of clinical pharmaceutical industry experience, including demonstrated clinical project management skills and competencies; alternatively, more than 5 years of supervisory experience in a healthcare setting plus 6 years of clinical research experience in the pharmaceutical or CRO industries.
• Demonstrated success managing or leading multidisciplinary project teams, with thorough knowledge of project management processes and experience using project management software.
• Strong financial acumen, including an understanding of how to develop and manage project budgets, alongside effective negotiation and…