Senior Clinical Project Manager – Oncology

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

📋 Description

• Take the lead on clinical projects independently, adhering to the study budget and scope of work.

• Establish and meet contracted and financial objectives for projects.

• Conduct international trials as required.

• Act as the primary point of contact for clients, delivering exceptional customer service.

• Engage in proposal activities and deliver client presentations.

• Communicate with project teams and senior management, including C-level stakeholders, at Precision and sponsor organizations.

• Oversee all components of clinical research trials.

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

• Create project status updates for clients and management.

• Identify key deliverables, performance metrics, and escalation points.

• Contribute to the effective management and execution of trials.

• Prepare and review protocols and study documentation, which includes project plans, informed consents, site contracts, and budgets.

• Provide comprehensive oversight for global or regional Phase I–IV oncology trials, ensuring adherence to timelines, scope, costs, and quality standards.

• Manage client relationships, project teams, budgets, and timelines throughout the entire study lifecycle.

⛳️ Requirements

• A degree or a related life science qualification, or an equivalent combination of education and experience.

• Previous experience in a full-service/global project management role within the CRO industry.

• Significant clinical operations experience within a CRO.

• At least 4 years of comprehensive project management experience in a clinical trial environment at a Clinical Research Organisation.

• Experience in managing studies within the oncology domain.

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

• Willingness and ability to travel domestically and internationally, including overnight stays.

• Proficient in written and spoken English communication.

• Strong presentation capabilities.

• Proficient in MS Office, MS Project, and PowerPoint.

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

• Ability to cultivate positive working relationships with both internal and external individuals and teams.

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

• Legally authorized 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 equal opportunity employment.

• Reasonable accommodations for applicants with disabilities.