Senior Project Manager – Oncology

Worldwide Clinical Trials

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

Posted 10/27/2026full-timeRemote • SpainSeniorWebsite

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 foster collaboration across global teams while implementing continuous improvement initiatives.

Highest-signal resume keywords

Clinical Project ManagementOncology ExperienceBudget ManagementICH-GCP GuidelinesProject Management Software

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Hard Skills

Clinical Trial ManagementProject PlanningRisk ManagementResource PlanningFinancial AcumenQuality AssuranceOperational EfficiencyMultidisciplinary Team LeadershipRegulatory ComplianceTime Management

Soft Skills

Conflict ResolutionCollaborationCustomer SatisfactionCommunicationMulticultural Team Management

Tools & Technologies

Project Management Software

Industry Keywords

Clinical ResearchPharmaceutical IndustryCRO EnvironmentLife SciencesHealthcare Supervisory Experience

About the role

Key responsibilities & impact

Lead the delivery of 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
Serve as the primary client contact and drive customer satisfaction
Identify project risks, evaluate operational challenges, and implement solutions
Foster collaboration and resolve conflicts across global and multicultural teams
Ensure project 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
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
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

Benefits

Comp & perks

Collaborative and inclusive work environment
Growth and career development opportunities
Opportunity to learn and shape the future of clinical research
Remote work
Domestic and international travel opportunities as needed