Senior Clinical Project Manager – Oncology

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

📋 Description

• Lead clinical projects independently in accordance 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 primary contact for clients and ensure high-quality customer service.

• Engage in proposal development and client presentations.

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

• Oversee all aspects of clinical research trials.

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

• Prepare project status reports, identify deliverables and performance metrics, and escalate issues as necessary.

• Contribute to the effective management and execution of trials.

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

• Provide comprehensive oversight for global and regional Phase I-IV oncology trials.

• Manage client relationships, project teams, budgets, timelines, scope, costs, and quality throughout the study lifecycle.

⛳️ Requirements

• A degree or a similar life science qualification, or a comparable combination of education and experience.

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

• Significant experience in Clinical Operations within a CRO setting.

• A minimum of 4 years of full-service Project Management experience in clinical trials at a Clinical Research Organisation.

• Experience managing studies specifically in 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 verbal communication in English.

• Strong presentation capabilities.

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

• Familiarity with 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 processes related to executing 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.

• Opportunities for team development.

• Support for professional growth.

• Equal Opportunity Employer.

• Reasonable accommodations for applicants with disabilities.