<div class="show-more-less-html__markup show-more-less-html__markup--clamp-after-5 relative overflow-hidden"> <p>Banook is an internationally recognised provider of reliable and innovative solutions supporting clinical trials worldwide.</p><p>Our German subsidiary is growing, and we are looking for a <strong>Project Manager</strong> to join our <strong>Clinical Operations</strong> team.</p><p>At Banook, we value teamwork, trust, and innovation — values that drive our mission to improve the quality and efficiency of clinical research across the globe.</p><p><br/></p><p><strong>The Role</strong></p><p><br/></p><p>As a <strong>Project Manager</strong>, you will oversee the full life cycle of clinical studies, from setup through to close-out, ensuring quality, compliance, and customer satisfaction.</p><p>You will act as the main point of contact for sponsors and internal teams, coordinating stakeholders across departments and time zones.</p><p>This position requires a professional who is highly organised, autonomous, and proactive, capable of managing multiple projects independently while maintaining strong communication with international colleagues.</p><p><br/></p><p><strong>Key Responsibilities</strong></p><ul><li>Coordinate all study-related communications and ensure clear alignment among stakeholders.</li><li>Lead the planning, execution, and delivery of clinical studies on time and within budget.</li><li>Monitor project performance, timelines, and risks to ensure successful study outcomes.</li><li>Prepare and maintain study documentation and specifications.</li><li>Ensure compliance with Banook’s Quality Management System (QMS) and applicable regulatory requirements.</li><li>Contribute to continuous improvement initiatives and support customer and regulatory audits.</li></ul><p><br/></p><p><strong>About You</strong></p><p>You are a motivated and detail-oriented professional who thrives in a dynamic environment. You enjoy taking ownership of your work and collaborating with international teams.</p><p><br/></p><p><strong>Qualifications and Experience:</strong></p><ul><li>Degree in Life Sciences, Biotechnology, Public Health, Pharmaceutical Sciences, or a related field.</li><li>At least 3 years’ experience as a Clinical Project Manager or Clinical Research Associate.</li><li>Strong understanding of local and international clinical research regulations.</li><li>Excellent communication skills in English (written and spoken).</li><li>Proficiency in project management and data analysis tools.</li></ul><p><br/></p><p><strong>Skills and Attributes:</strong></p><ul><li>Strong project planning and time management abilities.</li><li>Proven experience in budget management and risk assessment.</li><li>Excellent problem-solving and decision-making skills.</li><li>High level of ethics, integrity, and attention to detail.</li><li>Effective communication and stakeholder management.</li><li>Ability to work independently and demonstrate initiative.</li></ul><p><br/></p><p><strong>What We Offer</strong></p><ul><li>Salary package €65K–€67K</li><li>Up to two days of remote work per week.</li><li>Full reimbursement of public transport costs.</li><li>A dynamic, multicultural, and collaborative team environment.</li><li>The opportunity to contribute to meaningful work in the field of clinical research.</li></ul><p><br/></p> </div>