Clinical Project Manager

Minimum prerequisites Proven medical devices experience Based in Belgium or Spain Do You Recognize Yourself In Below Skills & Competences Comprehensive Clinical Trial Knowledge: in-depth understanding of study designs, operational processes, and regulations. Organizational & Time Management Expertise: skilled in efficiently managing complex projects, balancing multiple priorities, and meeting deadlines. Effective Communication: skilled in conveying project goals, updates, and requirements to stakeholders, ensuring clarity and alignment. Strategic Problem-Solving and Decision-Making: ability to analyze situations and make informed, timely decisions to address challenges. Team Leadership & Motivation: proven track record of leading, motivating, and supporting project teams to achieve high performance and successful outcomes. Stakeholder Engagement & Relationship Building: expertise in building strong, collaborative relationships with clients, vendors, and cross-functional teams to ensure project success. Flexibility & Attention to Detail: adapting to changing situations while ensuring precision and adherence to applicable international standards. Self-Directed & Proactive: takes responsibility over projects, initiating actions with minimal guidance. In This Role, You Will Have The Opportunity To Lead the planning, execution, and management of clinical studies. Collaborate closely with cross-functional teams and external partners to achieve study deliverables. Proactively identify clinical project risks, provide input for appropriate countermeasures and contingency plans, and assure implementation of action plans to reduce project risks. Monitor and manage project timelines, budgets, and resources effectively while maintaining a focus on integrity, transparency, and accuracy in reporting. Together with the team, ensure that program requirements are met and clinical studies are executed in a compliant and scientifically appropriate manner. Be highly involved in clinical study planning and study design. Involvement includes study deliverables such as clinical protocol, monitoring plan, and Trial Master Files. The Essential Requirements For The Job Include A Master of Science in a scientific, biological, or medical science field. Minimum of 3 years hands-on experience in clinical study conduct. Strong experience using Microsoft applications (Excel, Word, PowerPoint, Outlook). Multilingual proficiency can be advantageous for international trials. #J-18808-Ljbffr