Clinical Project Manager – Client Dedicated

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

📋 Description

• You will take the lead on clinical projects independently, adhering to the established budget and scope of work.

• Your strong interpersonal and organizational abilities will be utilized to set and meet objectives throughout project execution, including both contracted and financial goals.

• You may also oversee international trials as needed.

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

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

• 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.

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

• 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 documents, such as project plans, informed consents, site contracts, and budgets.

⛳️ Requirements

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

• Essential prior experience in a Global Clinical Project Management role within the CRO industry.

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

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

• Experience in managing studies related to Auto Immune Diseases.

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

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

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

• Strong presentation capabilities.

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

• Demonstrated ability to foster positive working relationships with individuals and teams, both internally and externally.

• A core understanding of medical terminology and clinical trial activities as they pertain to executing a clinical development plan.

🏝️ Benefits

• We offer a vibrant, high-energy team of dedicated members who thrive on challenges, attention to detail, and dynamic work environments.

• As a people-focused CRO, we provide a supportive and collaborative workplace that promotes work-life balance and encourages team development.