Clinical Project Manager

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

📋 Description

• You will take the lead on clinical projects, ensuring adherence to the study budget and scope of work independently.

• Your exceptional interpersonal and organizational abilities will be utilized to establish and meet objectives during project execution, covering both contractual and financial goals.

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

• Act as the primary liaison for clients, delivering outstanding 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 direct all facets of a clinical research trial or trials.

• Manage the project comprehensively across all functional areas, such as data management, safety, clinical, medical monitoring, and biostatistics.

• Create project status updates for clients and management, highlighting key deliverables, performance metrics for success, and any necessary escalations.

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

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

⛳️ Requirements

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

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

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

• Experience in managing studies within the Oncology field.

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

• Ability and willingness to travel domestically and internationally, including overnight stays.

• Proficient in English communication, both written and spoken.

• Strong presentation capabilities.

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

• Proven track record of developing positive working relationships with individuals and teams, both internally and externally.

• A solid understanding of medical terminology and clinical trial activities related to executing a clinical development plan.

🏝️ Benefits

• We provide an exhilarating high-energy atmosphere with dedicated, collaborative team members who enjoy challenges, excel in details, and thrive in dynamic environments.

• Our organization is a people-oriented CRO that fosters a supportive and collaborative environment, promoting work-life balance and encouraging team development.