Clinical Project Manager

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

📋 Description

• You will take the lead on clinical projects, ensuring they align with the study budget and scope of work.

• Utilizing your exceptional interpersonal and organizational skills, you will establish and meet objectives for project execution, which include both contracted and financial goals.

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

• Act as the primary liaison with clients to deliver outstanding customer service, participating 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 facets of a clinical research trial or multiple trials.

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

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

• Be an active member of the Project Team, focused on efficient trial management and execution.

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

⛳️ Requirements

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

• Essential to have 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 of full-service Project Management experience in a clinical trial environment for a Clinical Research Organisation.

• Experience in managing studies related to Oncology is required.

• A working understanding of GCP/ICH guidelines and the clinical development process is necessary.

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

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

• Strong presentation capabilities are a must.

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

• Demonstrated ability to foster positive working relationships with individuals and teams, both internally and externally.

• A solid understanding of medical terminology and clinical trial activities as they pertain to executing a clinical development plan is required.

🏝️ Benefits

• We provide a vibrant, high-energy, and dedicated team environment, where members embrace challenges, pay attention to detail, and thrive in dynamic settings.

• A supportive and collaborative atmosphere that promotes work-life balance and encourages team development.