Senior Clinical Project Manager – Oncology

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

📋 Description

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

• Establish and achieve objectives related to project execution and financial performance.

• Conduct international trials as necessary.

• 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 executives.

• Oversee all elements of clinical research trials.

• Manage all functional domains such as data management, safety, clinical operations, medical monitoring, and biostatistics.

• Generate project status reports for clients and management.

• Identify key deliverables, performance metrics, and necessary escalations.

• Assist in the effective management and execution of trials.

• Draft and review protocols and study documentation, encompassing project plans, informed consent forms, site contracts, and budgets.

• Handle client relationships, project teams, budgets, timelines, scope, costs, and quality for global/regional Phase I–IV oncology trials.

⛳️ Requirements

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

• Prior experience in a comprehensive/global Project Management role within the CRO industry.

• Significant Clinical Operations experience in a CRO setting.

• 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 within the field of Oncology.

• Familiarity with GCP/ICH guidelines and the clinical development process.

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

• Proficient in written and spoken English communication.

• Excellent presentation abilities.

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

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

• Capability to foster positive working relationships both internally and externally.

• Understanding of medical terminology and clinical trial processes necessary for executing a clinical development plan.

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

🏝️ Benefits

• A supportive and collaborative working environment.

• Emphasis on work-life balance.

• Opportunities for team development and growth support.

• Commitment to equal opportunity employment.

• Provision of reasonable accommodations during the application process.