Senior Clinical Project Manager – Oncology

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

📋 Description

• Lead clinical projects independently, adhering to the study budget and scope of work.

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

• Conduct international trials as required.

• Act as the primary liaison for clients, delivering exceptional customer service.

• Engage in proposal activities and deliver client presentations.

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

• Oversee all facets of clinical research trials.

• Manage all functional areas, including data management, safety, clinical operations, medical monitoring, and biostatistics.

• Prepare project status updates for clients and management, detailing deliverables, success metrics, and any escalations.

• Actively contribute to 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.

• Supervise clinical project delivery, functional departments, timelines, scope, cost, and quality across global/regional Phase I–IV oncology trials.

• Manage client relationships, project teams, budgets, and timelines throughout the entire study cycle, from proposal strategy and costing to completion.

⛳️ Requirements

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

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

• Extensive experience in Clinical Operations within a CRO.

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

• Experience in managing studies related to Oncology.

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

• Ability to drive and be available for domestic and international travel, including overnight stays.

• Proficient in written and spoken English communication.

• Strong presentation abilities.

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

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

• Proven capability to cultivate positive working relationships both internally and externally.

• Fundamental understanding of medical terminology and clinical trial activities related 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 work with a global team.

• Commitment to equal opportunity employment.

• Reasonable accommodations available during the application process.