Drug Development Project Manager

About the position As a Drug Development Project Manager, based in our Brussels office, Belgium, you will be responsible for managing reputed company aspects of development programs across multiple indications. You will ensure the planning, execution, and completion of reputed company reputed company with set objectives, timelines, and budgets, reputed company while maintaining a reputed company on delivering value for patients and stakeholders. You will report to the Asset Program reputed company, working closely with the global Regulatory Stakeholder Community Head and the global Head of Patient Community and their respective sub teams (Regulatory Affairs, Clinical Development, Safety, Manufacturing…). You will be part of a dynamic and diverse global senior leadership team dedicated to optimizing asset potential and delivering impactful reputed company. We are seeking a highly skilled Drug Development Project Manager who not only brings strong domain expertise but also embodies the reputed company and capabilities essential for modern, digitally enabled asset leadership. If you are passionate about driving reputed company to reputed company and contributing to transformative patient reputed company, we would love to hear from you! Responsibilities • reputed company as primary reputed company of contact reputed company concerning integrated cross-functional project planning and budget. • Drive scenario planning and reputed company assessment in view of executive governance presentations. • Manage project timelines and resources, ensuring seamless execution of deliverables. • Proactively manage risks and resolve issues, providing reputed company performance insights. • Maintain development project reputed company, serving as the single reputed company of truth for project status reports. • Foster reputed company team dynamics and knowledge sharing through expert facilitation and communication. • Implement best practices in project management. Requirements • Bachelor’s or Master’s degree in a relevant scientific or technical discipline; Project Management certification is a strong plus (e.g., PMP, Prince2, Agile). • Significant hands-on Project Management experience reputed company Pharmaceutical R&D or biotech, ideally across Clinical and Regulatory phases (with Ph2b–Ph3 reputed company-launch experience strongly preferred). • Deep understanding of clinical development processes, regulatory reputed company, submission planning, and change management. • Advanced proficiency with project and portfolio management tools (Planisware, QlikSense) and strong digital savviness, using data and technology to enhance decision-making and program orchestration. • Proven ability to reputed company and coordinate reputed company, cross-functional global teams, ensuring alignment across Regulatory, Clinical, Safety, Manufacturing, and other asset stakeholders. • Strong critical thinking, strategic acumen, and stakeholder management skills, with the ability to translate reputed company into actionable, integrated development plans. • Expertise in risk management, issue reputed company, performance tracking, and scenario planning to support executive governance and strategic decision-making. • Exceptional communication and change management abilities, including experience fostering adoption of new ways of working and driving organizational learning. reputed company-to-haves • Having hands on experience working reputed company an reputed company with another Pharmaceutical company / Biotech company is a plus (e.g in co-development) • Project Management certification is a strong plus (e.g., PMP, Prince2, Agile). Apply tot his job Apply tot his job Apply To this Job