Senior Clinical Project Manager – Oncology

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

📋 Description

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

• Establish and fulfill contractual and financial objectives related to the project.

• When necessary, manage international clinical trials.

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

• Engage in proposal activities and deliver client presentations.

• Coordinate with project teams, senior management, sponsors, and C-level stakeholders.

• Oversee all elements of clinical research trials.

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

• Prepare updates on project status, key deliverables, performance metrics, and any necessary escalations.

• Contribute to the effective management and execution of clinical trials.

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

• Coordinate with cross-functional internal and external stakeholders to ensure high study quality.

• Oversee the delivery of clinical projects, including timelines, scope, costs, and quality across global or regional Phase I–IV oncology trials.

• Participate in proposal strategy, development, costing, bid defense, and the comprehensive completion of studies.

• Manage relationships with clients, project teams, budgets, and timelines.

⛳️ Requirements

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

• Prior experience in a global Project Management role within the CRO industry.

• Significant experience in Clinical Operations at a CRO.

• A minimum of 4 years of comprehensive Project Management experience in a clinical trial environment with a Clinical Research Organization.

• Experience in managing studies in the field of Oncology.

• Familiarity with GCP/ICH guidelines and the clinical development process.

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

• Proficient in written and spoken English communication.

• Excellent presentation skills.

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

• Knowledge of software such as CTMS, eTMF, EDC, and IXRS.

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

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

• Must have legal authorization to work in the country of employment without employer sponsorship.

🏝️ Benefits

• A supportive and collaborative work environment.

• Emphasis on work-life balance.

• Opportunities for team development.

• An Equal Opportunity Employer.

• Reasonable accommodations available for applicants with disabilities.