Clinical Project Manager / Senior Clinical Project Manager

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

📋 Description

• You will take the lead on clinical projects independently, ensuring adherence to the study budget and scope of work.

• Utilize your exceptional interpersonal and organizational skills to establish and meet objectives during project execution, encompassing both contracted and financial goals.

• Act as the main point of contact for 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.

• Ensure comprehensive project management across all functional areas, such as data management, safety, clinical, medical monitoring, and biostatistics.

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

• Be an active member of the Project Team, contributing to the effective management and execution of trials.

• Draft and review protocols and other study documents, including project plans, informed consents, site contracts, and budgets.

⛳️ Requirements

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

• Essential prior experience in a full-service/global Project Management role within the CRO industry.

• Extensive background in Clinical Operations within a CRO, with a minimum of 4 years of full-service Project Management experience in a clinical trial setting for a Clinical Research Organisation.

• Experience in managing studies in the field of Oncology.

• 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 capabilities.

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

• Proven ability to foster 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

• We provide a vibrant, high-energy environment with dedicated, collaborative team members who relish challenges, pay attention to details, and excel in dynamic settings.

• A supportive and cooperative atmosphere that promotes work-life balance and encourages team development.