Clinical Project Manager

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

📋 Description

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

• Your strong interpersonal and organizational skills will be utilized to set and achieve objectives during project execution, including both contracted and financial goals.

• There may be opportunities for you to manage international trials as well.

• Act as the primary liaison with clients, delivering outstanding customer service, which includes involvement 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 manage all facets of clinical research trials.

• Ensure total project management across all functional areas such as data management, safety, clinical, medical monitoring, and biostatistics.

• Prepare project status updates for clients and management by identifying key deliverables and performance metrics for success and escalation.

• Be an active participant in the Project Team, contributing to the efficient management and execution of trials.

• Prepare and review protocols and other study documentation, including project plans, informed consents, site contracts, and budgets.

⛳️ Requirements

• A degree or a comparable 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.

• 5 to 7 years of industry experience, with at least 4 years in full-service Project Management within a clinical trial environment for a Clinical Research Organisation.

• Experience in managing studies within the Oncology field.

• A working knowledge of GCP/ICH guidelines and the clinical development process.

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

• Effective communication skills in English, both written and spoken.

• Strong presentation abilities.

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

• Demonstrated capacity to build 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 the execution of a clinical development plan.

🏝️ Benefits

• We provide an energetic, dedicated, and collaborative team environment where members relish challenges, pay attention to details, and thrive in dynamic settings.

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

• We aim to ensure that employees feel valued for their contributions every single day.