
Clinical Project Manager – Client Dedicated
Posted Jul 21

Posted Jul 21
This is a fully remote position, open to applicants in Hungary.
• You will take the lead on clinical projects independently, ensuring adherence to the study budget and scope of work.
• Act as the main point of contact for clients, delivering exceptional customer service, which includes engaging in proposal activities and client presentations.
• Collaborate with the Project Team and senior management from both Precision and sponsors, including C-level executives.
• Manage and oversee every facet of a clinical research trial or multiple trials.
• Ensure total project management across all functional areas, including data management, safety, clinical oversight, medical monitoring, and biostatistics, among others.
• Prepare project status updates for clients and management, highlighting key deliverables, performance metrics, and escalation points.
• Actively participate as a member of the Project Team, aiming to enhance the effective management and execution of trials.
• Draft and review protocols and other study documentation such as project plans, informed consents, site contracts, and budgets.
• A degree or a related qualification in life sciences, or an equivalent combination of education and experience.
• Essential prior experience in a Global Clinical Project Management role within the CRO industry.
• Experience managing Global studies, particularly those conducted in the LATAM region.
• Significant experience in Clinical Operations within a CRO, with at least 4 years in Clinical Project Management, ideally in a client-dedicated or FSP model.
• Background in managing studies related to Auto Immune Diseases.
• A solid understanding of GCP/ICH guidelines and the clinical development process.
• Willingness and ability to travel domestically and internationally, including overnight stays.
• Proficient communication skills in English, both written and spoken.
• Strong presentation abilities.
• Demonstrated computer proficiency (MS Office, MS Project, PowerPoint) and familiarity with software tools (CTMS, eTMF, EDC, IXRS).
• Proven capacity to build positive working relationships with individuals and teams, both internally and externally.
• A clear understanding of medical terminology and clinical trial activities as they pertain to the execution of a clinical development plan.
• We offer a vibrant, high-energy work environment with dedicated team members who thrive on challenges, pay attention to detail, and excel in dynamic settings.
• Emphasize work-life balance and support team development.
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