OverviewAt the heart of QIAGEN’s business is a vision to make improvements in life possible.We are on an exciting mission to make a real difference in science and healthcare. We are still the entrepreneurial company we started out as and have today achieved a size where we can bring our full power to many initiatives and to our presence across the globe.Our most valuable assets are our employees – around 6000 in over 35 locations worldwide. Our ambition is to have outstanding and passionate people working in the best teams, and we are constantly seeking new talent to join us.Few players have shaped the world of modern science and healthcare as much as QIAGEN, and our journey has only just begun.If you are looking to advance your career, seek new challenges and opportunities, enjoy working in dynamic, international, and diverse teams, and want to make a real impact on people’s lives, then QIAGEN is where you need to be.Join us. At QIAGEN, you make a difference every day.Position DescriptionThis is a global role, based within Europe, with main locations in the UK, Poland, France, and Spain. The position can be home-based.The role involves managing a team of Clinical Study Leads to deliver clinical studies on new infectious disease diagnostic assays and platforms. The role may also involve direct management of studies. Working cross-functionally with internal and external stakeholders is essential to ensure high-quality studies are completed on time and within budget. Leadership and management activities include team development, resource planning, management of clinical tasks (strategy, budgeting, planning, execution), and process improvement. The role-holder will leverage their expertise in infectious diseases and clinical affairs to define clinical strategy and uphold the scientific integrity of studies.Key responsibilities :
Manage the delivery of infectious disease diagnostic studies within the specific business area, ensuring excellence in planning and budgeting.Lead and manage the Clinical Study Leads team, fostering talent development and establishing a framework for team growth.Continuously evaluate clinical processes to maximize compliance and efficiency, adapting to changing regulations and guidance documentation related to clinical affairs.Develop clinical strategies and apply scientific knowledge to ensure the collection of high-quality clinical data.Position RequirementsUniversity degree or equivalent in a health-related field;
advanced degrees preferred.Minimum of 5 years’ experience in the in vitro diagnostic devices industry;
experience in clinical affairs is essential. Experience in other devices or pharmaceuticals is considered.Background in infectious diseases.Proven experience in direct line management and influential leadership, capable of leading without authority to influence decisions and ensure optimal clinical study outcomes within multifunctional teams. Strong rapport-building skills are required.Experience managing multiple high-priority projects across various sites.Excellent knowledge of the in vitro diagnostic industry, including product development processes (ISO13485), CLSI guidance, and ICH GCP is highly desirable.Willingness and ability to travel internationally approximately 15-20% of the time.What we offerAt QIAGEN, our people drive our success. We foster a passionate, innovative, and collaborative environment that encourages continuous improvement. We are committed to creating a diverse, inclusive workplace where everyone can thrive. We promote accountability, entrepreneurial decision-making, and support your growth to help shape the future of QIAGEN.QIAGEN is an equal opportunity employer. All qualified applicants will receive consideration without regard to race, color, sex, age, national origin, religion, sexual orientation, gender identity, veteran status, or disability.
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