Clinical Project Manager – Client Dedicated

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

📋 Description

• Lead clinical projects autonomously, adhering to the study budget and scope of work.

• Utilize strong interpersonal and organizational abilities to set and achieve objectives throughout project execution.

• Act as the main point-of-contact liaison with clients, ensuring exceptional customer service.

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

• Oversee and manage all components of clinical research trials.

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

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

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

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

⛳️ Requirements

• A degree or a comparable 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 in managing Global studies, particularly those in the LATAM region.

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

• Background in managing studies related to Auto Immune Diseases.

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

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

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

• Strong presentation capabilities.

• Demonstrated computer proficiency (MS Office, MS Project, PowerPoint) and familiarity with software tools (CTMS, eTMF, EDC, IXRS).

• Proven track record of cultivating 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 executing a clinical development plan.

🏝️ Benefits

• We provide an energetic and dedicated team environment where members enjoy challenges, thrive on attention to detail, and excel in dynamic settings.

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