Senior Clinical Project Manager – Oncology

This is a fully remote position, open to applicants in Hungary.

📋 Description

• Take charge of clinical projects autonomously in alignment with the study budget and defined scope of work

• Establish and meet project execution and financial targets

• Conduct international trials as necessary

• Act as the main point of contact for clients and deliver exceptional customer service

• Engage in proposal activities and client presentations

• Coordinate with project teams, senior management, and sponsors, including C-level executives

• Oversee all components of clinical research trials

• Manage various functional areas such as data management, safety, clinical operations, medical monitoring, and biostatistics

• Prepare updates on project status, identify deliverables and success metrics, and escalate any issues

• Actively contribute to efficient trial management and execution as a committed project team member

• Draft and review protocols and study documentation, which includes project plans, informed consent forms, site contracts, and budgets

• Oversee client relationships, project teams, budgets, timelines, scope, costs, and quality across global and regional Phase I–IV oncology trials

⛳️ Requirements

• A degree or equivalent qualification in life sciences, or a comparable mix of education and experience

• Prior experience in a full-service/global Project Management role within the CRO industry

• Significant Clinical Operations experience in a CRO setting

• Minimum of 4 years of comprehensive Project Management experience in a clinical trial environment, specifically within a Clinical Research Organisation

• Experience in managing oncology studies

• Working knowledge of GCP/ICH guidelines and the clinical development process

• Willingness to travel domestically and internationally, including overnight stays

• Proficient in written and verbal communication in English

• Excellent presentation skills

• Strong computer skills in MS Office, MS Project, and PowerPoint

• Familiarity with software such as CTMS, eTMF, EDC, and IXRS

• Demonstrated ability to foster positive working relationships with individuals and teams both internally and externally

• Fundamental understanding of medical terminology and clinical trial processes as related to the execution of a clinical development plan

• Candidates must possess legal authorization to work in the country of employment without requiring employer sponsorship

🏝️ Benefits

• Supportive and collaborative work environment

• Emphasis on work-life balance

• Opportunities for team development

• Commitment to being an Equal Opportunity Employer

• Reasonable accommodation support for applicants with disabilities