Clinical Project Manager – Client Dedicated

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

📋 Description

• Lead clinical projects independently, ensuring alignment with the study budget and scope of work.

• Utilize strong interpersonal and organizational abilities to establish and meet objectives during project execution.

• Act as the primary liaison with clients, delivering outstanding customer service, which includes involvement in proposal activities and client presentations.

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

• Oversee and manage all facets of clinical research trials.

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

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

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

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

⛳️ Requirements

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

• Prior experience in a Global Clinical Project Management role within the CRO industry is essential.

• Proven experience managing Global studies, including those in the LATAM region.

• Extensive background in Clinical Operations within a CRO, with at least 4 years of Clinical Project Management experience, preferably in a client-dedicated or FSP model.

• Experience in managing studies related to Auto Immune Diseases.

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

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

• Proficient in both written and spoken English communication.

• Excellent presentation skills.

• Proven computer proficiency (MS Office, MS Project, PowerPoint) and familiarity with software tools (CTMS, eTMF, EDC, IXRS).

• Demonstrated capability to build positive working relationships with individuals and teams, both internally and externally.

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

🏝️ Benefits

• A vibrant, energetic, and collaborative team of dedicated members.

• Promotion of work-life balance and encouragement of team development.