Clinical Project Manager / Senior Clinical Project Manager

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

📋 Description

• Take the lead on clinical projects while adhering to the study budget and defined scope of work.

• Utilize strong organizational and interpersonal skills to establish and meet objectives for project execution, including both contractual and financial goals.

• Act as the primary liaison for clients, delivering outstanding customer service, which includes involvement in proposal development 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 a clinical research trial or multiple trials.

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

• Create and present project status updates to clients and management, highlighting key deliverables, success metrics, and any necessary escalations.

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

• Draft and review protocols and other essential study documents, such as project plans, informed consent forms, site contracts, and budgets.

⛳️ Requirements

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

• Essential prior experience in a comprehensive/global Project Management role within the CRO sector.

• Significant experience in Clinical Operations within a CRO, with a minimum of 4 years of full-service Project Management experience in a clinical trial environment at a Clinical Research Organisation.

• Experience in managing studies specifically within Oncology.

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

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

• Proficient in effective communication in English, both written and verbal.

• Strong presentation abilities.

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

• Proven capability to cultivate positive working relationships with individuals and teams, both internally and externally.

• A thorough understanding of medical terminology and clinical trial processes as they relate to the execution of a clinical development plan.

🏝️ Benefits

• Work-life balance.

• Collaborative environment.

• Support for professional development.