Senior Clinical Project Manager – Oncology

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

📋 Description

• Take the lead on clinical projects while adhering to the study's budget and scope of work.

• Establish and meet contracted and financial project goals.

• Conduct international trials as required.

• Act as the main point of contact for clients, ensuring exceptional customer service.

• Engage in proposal initiatives and client presentations.

• Collaborate with project teams and senior management, including C-suite stakeholders.

• Oversee all facets of clinical research trials.

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

• Generate project status updates for clients and management.

• Identify key deliverables, success metrics, and escalation requirements.

• Contribute to the effective management and execution of trials.

• Draft and review protocols and study documents, which include project plans, informed consents, 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 equivalent life science qualification, or a comparable mix of education and experience.

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

• Significant experience in Clinical Operations within a CRO environment.

• A minimum of 4 years of full-service Project Management experience in a clinical trial setting for a Clinical Research Organization.

• Experience in managing studies in the field of Oncology.

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

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

• Proficient in written and spoken English communication.

• Strong skills in presentation delivery.

• Demonstrated computer proficiency: MS Office, MS Project, and PowerPoint.

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

• Ability to cultivate positive working relationships both internally and externally.

• 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.

• Encouragement for team development.

• Equal Opportunity Employer.

• Reasonable accommodations available for applicants with disabilities.