Clinical Project Manager

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

📋 Description

• Are you a seasoned full-service Project Manager in the clinical trials sector, dedicated to tackling the challenges in the research and development of innovative compounds in Oncology?

• You will autonomously manage clinical projects in alignment with the study budget and defined scope of work.

• Utilize your exceptional interpersonal and organizational skills to establish and fulfill objectives in project execution, including both contracted and financial goals.

• Act as the primary liaison with the client to deliver outstanding customer service, which includes involvement in proposal initiatives and client presentations.

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

• Oversee and direct all facets of clinical research trials.

• Manage all functional areas of the project, encompassing data management, safety, clinical oversight, medical monitoring, and biostatistics.

• Compile project status reports for clients and management, identifying key deliverables and success metrics, and addressing any escalations.

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

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

⛳️ Requirements

• A degree or a relevant qualification in life sciences, or a comparable combination of education and experience.

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

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

• Experience in managing studies in the field of Oncology.

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

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

• Effective communication skills in English, both written and verbal.

• Strong presentation abilities.

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

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

• A solid understanding of medical terminology and clinical trial processes as they relate to executing a clinical development plan.

🏝️ Benefits

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

• Precision for Medicine's uniquely integrated approach facilitates the science of precision medicine by combining innovative clinical trial designs, industry-leading operational and medical expertise, advanced biomarker and data analytics solutions, and a genuine passion for rare diseases and oncology.

• We are a people-focused CRO that fosters a supportive and collaborative atmosphere, promoting work-life balance and encouraging team development.

• We are committed to ensuring that employees feel valued for their daily contributions.