Senior Clinical Project Manager – Oncology

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

📋 Description

• Lead clinical projects autonomously in alignment with the study budget and scope of work.

• Establish and meet contractual and financial objectives for projects.

• Conduct international trials as required.

• Act as the main client liaison and deliver exceptional customer service.

• Engage in proposal activities and present to clients.

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

• Oversee all elements of clinical research trials.

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

• Prepare project status updates, define deliverables and success metrics, and escalate issues as necessary.

• Contribute to the effective management and implementation of trials.

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

⛳️ Requirements

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

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

• Extensive experience in Clinical Operations within a CRO.

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

• Experience in managing studies related to Oncology.

• Solid understanding of GCP/ICH guidelines and the clinical development process.

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

• Strong written and verbal communication skills in English.

• Excellent presentation abilities.

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

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

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

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

• Legally permitted 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 and growth support.

• Equal Opportunity Employer.

• Reasonable accommodations available for applicants with disabilities.