Marike Thie

Marike Thie currently excels as a Clinical Project Manager II at Allucent, where she leverages over a decade of experience in clinical research to drive the successful execution of complex clinical trials. Her role involves meticulous planning and oversight of studies in accordance with ICH-GCP guidelines and applicable regulatory requirements, ensuring the highest standards of compliance and quality. Marike’s expertise spans across multiple therapeutic areas, with a particular focus on oncology, where she has contributed to numerous Phase I and II clinical trials, including study start-ups, site management, and data collection processes.

At Allucent, Marike plays a pivotal role in coordinating cross-functional teams across departments such as Clinical Start-Up, Medical Affairs, Pharmacovigilance, Data Management, and Biostatistics. Her strong organizational skills and proactive communication facilitate seamless collaboration, enabling the timely initiation and completion of studies. She is adept at timeline planning and implementation, utilizing tools like CTMS and EDC systems to monitor progress and ensure adherence to project milestones.

Marike’s key projects often involve complex study start-up activities, including site qualification, regulatory submissions, and contract negotiations, which demand her comprehensive knowledge of SOPs and clinical research regulations. Her resilience and team spirit foster a collaborative environment, essential for navigating the challenges of global clinical trials. With her expertise in project management, pharmacovigilance, and clinical research operations, Marike Thie continues to contribute significantly to advancing innovative therapies and ensuring the integrity and success of each study she manages.