Clinical Project Manager / Senior Clinical Project Manager

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

📋 Description

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

• Utilize your strong interpersonal and organizational abilities to establish and meet objectives in project execution, including both contracted and financial goals.

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

• Collaborate with the Project Team and senior management from both Precision and sponsors, 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.

• Prepare project status updates for clients and management, identifying 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.

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

⛳️ Requirements

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

• Essential prior experience in a full-service/global Project Management role within the CRO industry.

• Extensive background in Clinical Operations within a CRO, with at least 4 years of comprehensive Project Management experience in a clinical trial environment for a Clinical Research Organization.

• Experience managing studies in the field of Oncology.

• A working knowledge 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 spoken.

• Strong presentation abilities.

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

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

• A solid understanding of medical terminology and clinical trial activities as they relate to implementing a clinical development plan.

🏝️ Benefits

• Join an energetic, dedicated, and collaborative team that thrives on challenges, pays attention to details, and excels in dynamic environments.

• Work in a supportive and collaborative atmosphere that promotes work-life balance and encourages team development.

• Opportunities for professional growth and development.