WT
Senior / Project Manager - Oncology (Europe)
Contract type
Ongoing
Work mode
Remote · Europe
Experience
Senior · 5+ years
Job description
A Senior/Project Manager role at a global CRO, leading Phase I-IV clinical trials from start-up through closeout for local, regional and global studies. The role is responsible for on-time, on-budget, high-quality delivery and serves as the central coordination point across teams, clients and partners.
At a glance
- Work mode
- Remote · Europe
- Languages
- English – fluent
What you'll do
- Lead the delivery of Phase I-IV clinical trials from study start-up through closeout, ensuring successful execution across all project phases.
- Direct cross-functional project teams and coordinate internal stakeholders, clients, vendors, and subcontractors to achieve project objectives.
- Develop, maintain, and adapt project plans, timelines, and resource strategies to support study success.
- Manage project budgets and financial performance, ensuring delivery aligns with contractual commitments and business goals.
- Serve as the primary client contact, building strong relationships and driving high levels of customer satisfaction.
- Identify project risks, evaluate complex operational challenges, and implement effective solutions to keep studies on track.
- Foster a collaborative team environment, resolving conflicts and supporting team effectiveness across global and multicultural settings.
- Ensure all project deliverables meet quality, timeline, regulatory, and client expectations.
- Drive continuous improvement initiatives that enhance operational efficiency and the quality of project execution.
What we're looking for
- University or college degree, preferably in Life Sciences, or qualification in a related allied health profession; equivalent combinations of education and experience will also be considered.
- At least 5 years of clinical pharmaceutical industry experience, including proven Oncology clinical project management experience; alternatively, significant healthcare supervisory and clinical research experience within pharmaceutical or CRO environments.
- Demonstrated success leading multidisciplinary and cross-functional project teams in a clinical research setting.
- Strong knowledge of project management principles, including time, quality, cost, resource planning, and risk management.
- Solid financial acumen, including experience developing and managing project budgets.
- Thorough understanding of ICH-GCP guidelines and international regulatory requirements for clinical development programs.
- Experience using project management software and the ability to manage multiple priorities in a fast-paced environment.
- Proficiency in English, both written and verbal. Fluency in the local office language is also required.
Apply
About Worldwide Clinical Trials
Join a global Contract Resource Organization (CRO) where innovation meets purpose.
A global Contract Resource Organization (CRO) with more than 4,000 professionals across the globe, fostering a collaborative and inclusive environment where diverse perspectives are valued, growth is encouraged, and every contribution makes an impact.
Mission
We're driven by a shared commitment to improving lives through high-quality clinical research.
Key facts
- more than 4,000 professionals
- Clinical research (CRO)
- More than 4,000 professionals across the globe
- Global Contract Resource Organization (CRO)
What they value
- Collaborative and inclusive environment
- Diverse perspectives are valued
- Growth is encouraged