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    Mieke Borgs

    Head Clinical Operations Europe at BeiGene

    Professional Background

    Mieke Borgs is a highly accomplished professional in the field of biomedical sciences. With an extensive career spanning over two decades, she has held a variety of prominent roles at leading pharmaceutical companies. Currently, Mieke serves as the Head of Clinical Operations Europe at BeiGene, where she is at the forefront of clinical trial management and operations. Her leadership ensures that the clinical trials are conducted smoothly and efficiently, ultimately contributing to the advancement of innovative therapies that improve patient outcomes.

    Before her tenure at BeiGene, Mieke spent a significant portion of her career at Novartis, where she held multiple high-level positions. Notably, she was the Global Head of Clinical Document Governance and Management, where she played an instrumental role in establishing best practices for the management of clinical documentation involving drug development processes. In addition, she led the Global Head Trial Management Center of Excellence and provided strategic oversight and operational excellence to various oncology projects. Her deep expertise and leadership at Novartis have greatly contributed to the successful execution of numerous clinical trials that have impacted cancer treatment options worldwide.

    Mieke previously excelled as the Global Head of Functional Excellence in Oncology, where she oversaw the development and implementation of innovative functional strategies within the organization. Her role included managing cross-functional teams, optimizing clinical trial processes, and ensuring alignment on project objectives. Her impactful work at Novartis has solidified her reputation as a leading authority in clinical operations and research.

    Prior to her distinguished career at Novartis, Mieke worked at F. Hoffmann La Roche Ltd, where she took on various roles that added depth to her clinical research expertise. She served as the Operations Project Leader, Studies Leader, and Global Study Manager, leading complex clinical trials while ensuring adherence to regulatory standards and delivering results in a timely manner. Mieke's early experience as a Clinical Research Scientist and CRA/CRM at Janssen Pharmaceutica provided her with a strong foundation in clinical research methodologies and compliance requirements, enabling her to navigate the complexities of the pharmaceutical industry effectively.

    Education and Achievements

    Mieke Borgs earned her Doctor of Philosophy (PhD) in Biomedical Sciences from the prestigious Katholieke Universiteit Leuven. Her in-depth academic training provided her with a solid scientific background, equipping her with the knowledge and skills necessary to excel in her career in clinical operations. Mieke's education has been instrumental in her ability to lead teams and contribute to the development of groundbreaking therapies.

    Throughout her career, Mieke has achieved numerous significant milestones that highlight her expertise and commitment to advancing medical research. Her leadership in clinical operations has been recognized within the industry, and she has played a key role in ensuring that important therapeutic products progress from initial conception through clinical development stages successfully.

    Achievements

    Mieke Borgs is recognized not only for her professional roles but also for her ability to cultivate strong relationships with internal and external stakeholders, enhancing collaboration across diverse teams. Her commitment to operational excellence and her deep understanding of the clinical research environment make her a sought-after expert in her field.

    By leading teams that are integral to clinical operations in oncology, Mieke has significantly contributed to the advancement of therapies that target various cancers. Her work has often centered around optimizing trial processes and harnessing innovative methodologies to ensure clinical trials are efficient and compliant with industry standards. Mieke's insights into clinical document governance have provided essential frameworks for ensuring data integrity and regulatory compliance, vitally important aspects in clinical research.

    With a career forged in some of the largest and most respected organizations within the pharmaceutical industry, Mieke Borgs continues to influence the future of clinical research and operations in Europe and beyond. Her academic excellence, professional experience, and leadership qualities place her at the apex of her field, making her an inspiring figure for those in the biomedical sciences arena.

    Related Questions

    How did Mieke Borgs apply her PhD in Biomedical Sciences to her roles in clinical operations?
    What strategies has Mieke Borgs implemented at BeiGene to enhance clinical trial efficiency in Europe?
    What were some of the key contributions Mieke Borgs made during her time at Novartis?
    How does Mieke Borgs' expertise in clinical document governance improve clinical trial processes?
    What challenges has Mieke Borgs faced in her career, and how did she overcome them?
    Mieke Borgs
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    Location

    Basel, Basel, Switzerland