Clinical Project Manager – Client Dedicated

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

📋 Description

• Take charge of clinical projects independently, ensuring they align with the study budget and scope of work.

• Utilize excellent interpersonal and organizational abilities to establish and meet goals in project execution, focusing on both contracted and financial objectives.

• Act as the main point of contact for 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.

• Oversee and manage all components of a clinical research trial or multiple trials.

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

• Prepare project status reports for clients and management, highlighting key deliverables and success metrics, along with any necessary escalations.

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

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

⛳️ Requirements

• A degree or a related life sciences qualification, 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, specifically within the LATAM region.

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

• Experience in managing studies related to Auto Immune Disease.

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

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

• Proficiency in effective communication in English, both written and verbal.

• Strong presentation abilities.

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

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

• A clear understanding of medical terminology and clinical trial activities in relation to the execution of a clinical development plan.

🏝️ Benefits

• We provide an exciting, high-energy, and dedicated team environment where members relish challenges, excel in detail, and thrive in dynamic settings.

• A supportive and collaborative workplace that fosters work-life balance and encourages team development.