Senior Clinical Project Manager – Oncology

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

📋 Description

• Independently oversee clinical projects in alignment with the study budget and scope of work.

• Establish and attain contracted and financial project goals.

• Conduct international trials as necessary.

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

• Engage in proposal activities and deliver client presentations.

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

• Manage and lead all facets of clinical research trials.

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

• Prepare updates on project status for clients and management.

• Identify key deliverables, performance metrics, and escalation points.

• Contribute to the effective management and execution of trials.

• Prepare and review protocols and study documentation, such as project plans, informed consents, site contracts, and budgets.

• Provide comprehensive oversight for global or regional Phase I–IV oncology trials, ensuring adherence to timelines, scope, cost, and quality.

⛳️ Requirements

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

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

• Extensive experience in Clinical Operations within a CRO environment.

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

• Experience in managing studies within the field of Oncology.

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

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

• Proficient in written and verbal communication in English.

• Strong presentation capabilities.

• Demonstrated computer proficiency: MS Office, MS Project, and PowerPoint.

• Familiarity with CTMS, eTMF, EDC, and IXRS.

• Proven 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.

• Legally authorized to work in the country of employment without employer sponsorship.

🏝️ Benefits

• Supportive and collaborative work environment.

• Emphasis on work-life balance.

• Encouragement for team development.

• Global team atmosphere.

• Equal Opportunity Employer.

• Reasonable accommodations available for the application process.