Senior Clinical Project Manager (Oncology)

Location: Remote, Spain. Candidates must be legally authorized to work in Spain without employer sponsorship. Domestic and international travel, including overnight stays, may be required.

Company

hirify.global is a contract research organization delivering clinical trial operations, precision medicine services, biomarker solutions, and data analytics for oncology and rare disease research.

What you will do

• Lead full-service Phase I–IV clinical projects in oncology in line with agreed scope, budget, timelines, and quality requirements.
• Oversee functional areas including data management, safety, clinical operations, medical monitoring, and biostatistics.
• Manage sponsor relationships as the primary client liaison, including proposal activities, presentations, and bid defence.
• Coordinate internal and external project teams and communicate with senior management and sponsor stakeholders, including C-level contacts.
• Prepare project status reports, monitor deliverables and performance metrics, and escalate risks and issues.
• Review protocols and prepare study documentation, project plans, informed consent forms, site contracts, and budgets.

Requirements

• Degree or equivalent qualification in life sciences, or an equivalent combination of education and experience.
• Previous full-service or global project management experience in the CRO industry, including at least four years managing clinical trials.
• Experience managing oncology studies and working in clinical operations within a CRO.
• Working knowledge of GCP/ICH guidelines, the clinical development process, medical terminology, and clinical trial activities.
• Professional English communication skills are required, and candidates must be legally authorized to work in Spain without employer sponsorship.
• Strong presentation, organizational, interpersonal, MS Office, MS Project, PowerPoint, CTMS, eTMF, EDC, and IXRS skills; ability to drive and travel domestically and internationally.

Culture & Benefits

• Supportive, collaborative, people-focused CRO environment.
• Work-life balance and opportunities for team development.
• Work with international clinical research programs and cross-functional stakeholders.
• Opportunity to contribute to the development of novel oncology and rare disease therapies.