At 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 asset are our employees – more than 6000 in over 35 locations around the world. Our ambition is to ensure we have outstanding and passionate people working in the best teams and we are constantly looking for new talent to join us. There are few players who have shaped the world of modern science and healthcare as much as QIAGEN, and we have only just started. If you are looking to advance your career, are seeking 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 Description This role within the Clinical Science team of Clinical Affairs will serve as a Clinical Expert contributing towards gathering clinical evidence and presenting it to regulatory bodies in support of the In-vitro Diagnostic (IVD) product range within QIAGEN, primarily focused on the Oncology and Companion Diagnostics portfolio. The post-holder is accountable for managing performance evaluation for IVDs as well as contributing to clinical strategy, study protocols, study reports and post market surveillance activity. The post-holder will coordinate the efforts and activities of diverse internal and external stakeholders, ensuring compliance with organizational SOPs and international regulations.
Key Responsibilities Managing the delivery of clinical/performance evaluation plans, scientific validity reports, and clinical/performance evaluation reports to support Global Clinical Affairs activities around medical device (MD)/IVD and Companion Diagnostics development, registration and marketing, ensuring accuracy of information, data and referencing for the documents produced.
Manage external contractors and vendors, ensuring projects are delivered within budget and to timeline.
Collaborate with internal project stakeholders (including but not limited to Medical Affairs, Product Development, Quality, Regulatory) and external partners.
Review/contribute to non-clinical QIAGEN documents and represent Clinical Affairs on multi-functional teams to ensure requirements are met for IVDR/FDA and ROW compliance.
Update, review and contribute to SOPs and drive continuous improvement within the Clinical Affairs team including training other staff and representing QIAGEN in industry working groups.
Position Requirements Please submit your application in English. Master's degree (preferably PhD) in Life Sciences with a minimum of 3 years' employment experience with in vitro diagnostic devices and/or a clinical setting.
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