Clinical Project Manager

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

📋 Description

• Are you a seasoned full-service Project Manager with expertise in clinical trials, focused on tackling the challenges associated with the research and development of innovative compounds in Oncology?

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

• Utilizing your exceptional interpersonal and organizational abilities, you will set and accomplish objectives throughout the project execution, encompassing both contracted and financial goals.

• Act as the main point of contact for clients, ensuring outstanding customer service, which includes involvement in proposal activities and client presentations.

• Coordinate with the Project Team and senior management at both Precision and sponsor organizations, including C-level executives.

• Manage all facets of one or more clinical research trials.

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

• Generate project status updates for clients and management, highlighting key deliverables, performance metrics, and any necessary escalations.

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

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

⛳️ Requirements

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

• Previous experience in a full-service/global Project Management role within the CRO industry is crucial.

• 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 Organization.

• Experience in managing studies specifically within Oncology.

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

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

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

• Strong presentation capabilities.

• Demonstrated computer skills (MS Office, MS Project, PowerPoint) and experience with software (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 processes as they relate to the execution of a clinical development plan.

🏝️ Benefits

• Health insurance

• 401(k) matching

• Flexible work arrangements

• Paid time off

• Professional development opportunities