Senior Clinical Project Manager – Oncology

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

📋 Description

• Oversee clinical projects in line with the study budget and defined scope of work.

• Establish and reach contracted and financial objectives for the project.

• Conduct international trials as necessary.

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

• Engage in proposal activities and deliver client presentations.

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

• Manage and lead all components of clinical research trials.

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

• Create project status updates for clients and management.

• Identify key deliverables, success metrics, and necessary escalations.

• Play an active role in the efficient management and execution of trials as a project team member.

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

• Manage client relationships, project teams, budgets, timelines, scope, cost, quality, and the overall delivery of clinical projects across global/regional Phase I–IV oncology trials.

• Engage in proposal strategy, development, costing, bid defense, and oversee studies until completion.

⛳️ Requirements

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

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

• Extensive Clinical Operations experience in a CRO setting.

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

• Experience managing studies in the field of Oncology.

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

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

• Proficient written and verbal communication skills in English.

• Strong presentation capabilities.

• Proven proficiency in MS Office, MS Project, and PowerPoint.

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

• Demonstrated ability to cultivate positive working relationships with individuals and teams, both internally and externally.

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

• Must be legally authorized to work in the country of employment without employer sponsorship.

🏝️ Benefits

• Supportive and collaborative work environment.

• Emphasis on work-life balance.

• Opportunities for team development and growth support.

• Chance to collaborate with a global team.

• Opportunities for domestic and international travel.

• Equal opportunity employment practices.

• Reasonable accommodations available for applicants with disabilities.