Senior Clinical Project Manager – Oncology

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

📋 Description

• Take charge of clinical projects independently, adhering to the study budget and defined scope of work.

• Establish and fulfill contracted and financial objectives for projects.

• Manage international trials as necessary.

• Act as the primary point of contact for clients, delivering outstanding customer service.

• Engage in proposal efforts and client presentations.

• Collaborate with project teams, senior management, sponsors, and C-level stakeholders.

• Oversee all facets of clinical research trials.

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

• Generate project status updates for clients and management.

• Identify essential deliverables, success metrics, and escalation points.

• 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/regional Phase I–IV oncology trials, ensuring compliance with timelines, scope, cost, and quality.

⛳️ Requirements

• A degree or equivalent 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 background in Clinical Operations within a CRO.

• Minimum of 4 years of full-service Project Management experience in a clinical trial environment at a Clinical Research Organisation.

• Experience in managing studies related to 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 proficiency in MS Office, MS Project, and PowerPoint.

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

• Ability to foster positive working relationships with individuals and teams both internally and externally.

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

• Legally permitted 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.

• Global team culture.

• Equal opportunity employer.

• Reasonable accommodations for applicants with disabilities.