Clinical Project Manager / Senior Clinical Project Manager

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

📋 Description

• Take charge of clinical projects independently, ensuring adherence to the study budget and scope of work.

• Utilize exceptional interpersonal and organizational skills to establish and accomplish objectives throughout project execution.

• Act as the main point of contact with clients, delivering outstanding customer service, which includes engaging in proposal activities and client presentations.

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

• Oversee and guide all components of clinical research trials.

• Manage the entire project across all functional areas, including data management, safety, clinical, medical monitoring, and biostatistics.

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

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

• Prepare and review protocols and additional study documentation, including 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 full-service/global Project Management role within the CRO industry.

• 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 Organization.

• Experience in managing studies in the field of Oncology.

• 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 abilities.

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

• Proven capacity to foster positive working relationships with individuals and teams both internally and externally.

• Established understanding of medical terminology and clinical trial activities as they pertain to the execution of a clinical development plan.

🏝️ Benefits

• We provide a vibrant, high-energy environment with dedicated, collaborative team members who relish challenges, excel in attention to detail, and thrive in dynamic settings.

• A supportive and collaborative atmosphere that fosters work-life balance and encourages team growth.

• Excellent opportunities for professional development and advancement.