Senior Project Manager – Oncology

Worldwide Clinical Trials

. Lead Phase I-IV clinical trials from study start-up through closeout .

Posted 10/14/2026full-timeRemote • United KingdomSeniorWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in leading Phase I-IV clinical trials, managing project budgets, and ensuring compliance with ICH-GCP guidelines. Proven ability to drive customer satisfaction and enhance operational efficiency through effective project management and cross-functional team leadership.

Highest-signal resume keywords

Oncology Clinical Project ManagementProject Management PrinciplesICH-GCP GuidelinesProject Budget ManagementCross-Functional Team Leadership

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Clinical Trial ManagementProject PlanningRisk ManagementResource PlanningBudget Management

Soft Skills

Conflict ResolutionCollaborationCustomer Satisfaction

Tools & Technologies

Project Management Software

Industry Keywords

Clinical ResearchPharmaceutical IndustryCRO EnvironmentsLife SciencesHealthcare Supervisory Experience

About the role

Key responsibilities & impact

Lead Phase I-IV clinical trials from study start-up through closeout
Direct cross-functional project teams and coordinate internal stakeholders, clients, vendors, and subcontractors
Develop, maintain, and adapt project plans, timelines, and resource strategies
Manage project budgets and financial performance in line with contractual commitments and business goals
Serve as the primary client contact and drive customer satisfaction
Identify project risks and implement solutions to keep studies on track
Foster collaboration and resolve conflicts across global and multicultural teams
Ensure deliverables meet quality, timeline, regulatory, and client expectations
Drive continuous improvement initiatives to enhance operational efficiency and project execution quality

Requirements

What you’ll need

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
Proven Oncology clinical project management experience, or significant healthcare supervisory and clinical research experience within pharmaceutical or CRO environments
Experience 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
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
Ability to manage multiple priorities in a fast-paced environment
Proficiency in English, written and verbal
Fluency in the local office language required

Benefits

Comp & perks

Diverse and inclusive work environment
Supportive and collaborative teams
Accessible leadership
Equal employment opportunities
Domestic and international travel opportunities