Senior Clinical Project Manager – Oncology

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

📋 Description

• Take charge of clinical projects independently in alignment with study budgets and scopes of work.

• Establish and fulfill contracted and financial project goals.

• Conduct international trials as required.

• Act as the main point of contact for clients while delivering exceptional customer service.

• Engage in proposal initiatives and present to clients.

• Collaborate with project teams and senior management, including C-level executives.

• Oversee all facets of clinical research trials.

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

• Prepare project status reports, identify deliverables and performance indicators, and escalate issues as necessary.

• Contribute to the efficient management and execution of trials.

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

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

⛳️ Requirements

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

• Prior experience in a full-service/global Project Management position within the CRO sector.

• Significant Clinical Operations experience within a CRO environment.

• At least 4 years of full-service Project Management experience in a clinical trial context working for a Clinical Research Organisation.

• Experience overseeing studies in the Oncology field.

• 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 verbal English communication.

• Strong skills in presentation.

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

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

• Capability to foster positive working relationships both internally and externally.

• Fundamental understanding of medical terminology and clinical trial operations related to executing a clinical development plan.

• 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.

• Encouragement for team development.

• Commitment to equal opportunity employment.

• Reasonable accommodations available for applicants with disabilities.