Senior Clinical Project Manager – Oncology

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

📋 Description

• Independently lead clinical projects in accordance with the study budget and defined scope of work.

• Establish and meet contracted and financial objectives for projects.

• Conduct international trials as necessary.

• Act as the main client liaison, 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.

• Manage and oversee all facets of clinical research trials.

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

• Prepare updates on project status for clients and management, highlighting deliverables, performance metrics, and any escalations.

• Play an active role in the Project Team to ensure efficient management and execution of trials.

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

• Oversee the delivery of clinical projects, functional departments, timelines, scope, costs, and quality across global or regional Phase I-IV oncology trials.

• Participate in the development of proposal strategy, costing, bid defense, and comprehensive study-cycle completion.

• Manage relationships with clients, project teams, budgets, and timelines.

⛳️ Requirements

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

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

• Extensive experience in Clinical Operations within a CRO.

• A 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.

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

• Willingness to travel domestically and internationally, including overnight trips.

• Proficient in written and spoken English communication.

• Strong presentation abilities.

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

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

• Proven capability to cultivate positive working relationships with internal and external individuals and teams.

• Solid understanding of medical terminology and clinical trial activities in relation to executing a clinical development plan.

• Must possess legal authorization 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.

• Equal Opportunity Employer.

• Reasonable accommodations for applicants with disabilities.