Clinical Project Manager

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

📋 Description

• Are you a seasoned Project Manager in the clinical trials domain, actively engaged in tackling the challenges associated with the research and development of innovative compounds in Oncology?

• In this crucial position, you will have comprehensive oversight of clinical projects across global and regional (ph I-IV) trials within the field of Oncology.

• You will be responsible for the successful delivery of clinical projects, overseeing all functional departments, and ensuring adherence to established timelines, scope, budget, and quality standards.

• Your involvement will span all phases of the study, from proposal strategy and development to costing and bid defense, managing studies through to completion while overseeing client relationships, project teams, budgets, and timelines.

• Collaboration with both internal and external stakeholders will be key, as you drive quality and coordinate the study team.

• You will independently manage clinical projects in line with the study budget and scope of work, leveraging your strong interpersonal and organizational skills to meet both contractual and financial objectives. There may also be opportunities to lead international trials.

• Act as the main point of contact for clients, delivering exceptional customer service, which includes participating in proposal activities and client presentations.

• Coordinate with the Project Team and senior management from both Precision and sponsors, including C-level executives.

• Oversee and guide all components of a clinical research trial or trials.

• Ensure total project management across all functional areas, including data management, safety, clinical operations, medical monitoring, and biostatistics.

• Prepare status updates for clients and management, identifying key deliverables, performance metrics for success, and escalation points.

• Actively participate as a member of the Project Team, aiming to enhance the management and execution of trials.

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

⛳️ Requirements

• A degree or a similar 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 is essential.

• A minimum of 5 to 7 years of industry experience, including at least 4 years of full-service Project Management experience in a clinical trial environment at a Clinical Research Organisation.

• Proven experience managing studies within the Oncology field.

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

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

• Proficiency in effective communication in English, both written and spoken.

• Strong presentation abilities.

• Demonstrated computer proficiency (MS Office, MS Project, PowerPoint) and software experience (CTMS, eTMF, EDC, IXRS).

• Proven capability to cultivate positive working relationships with individuals and teams, both internally and externally.

• A solid understanding of medical terminology and clinical trial activities as they pertain to the execution of a clinical development plan.

🏝️ Benefits

• Precision for Medicine's uniquely integrated offering enables the advancement of precision medicine by merging innovative clinical trial designs, leading operational and medical expertise, advanced biomarker and data analytics solutions, along with a genuine passion for rare diseases and oncology.

• A supportive and collaborative environment that fosters work-life balance and encourages team development.