Elizabeth M. Troll is a distinguished executive with over 42 years of global leadership experience in quality assurance, regulatory compliance, and operational excellence across the pharmaceutical, biopharmaceutical, and healthcare industries. With a career dedicated to ensuring the highest standards of quality management and governance, she has played a pivotal role in shaping compliance frameworks that align with regulatory requirements while optimizing business processes. Her expertise spans Quality Management Systems (QMS), vendor oversight, inspection readiness, leadership development, and mentorship, making her a trusted authority in driving quality-centric cultures within organizations.
Throughout her career, Liz has led strategic quality initiatives at top-tier organizations, including Endpoint Clinical, Novan Inc., QuintilesIMS, and Otsuka, where she was instrumental in developing and implementing global compliance programs. As Vice President of Quality at Endpoint Clinical, she spearheaded the company’s global quality strategy, overseeing clinical Quality Management Systems, product testing, and regulatory adherence while fostering a company-wide culture of quality improvement. At Novan Inc., she held leadership roles in quality assurance, ensuring compliance across Good Clinical Practice (GCP), Good Laboratory Practice (GLP), and Good Manufacturing Practice (GMP) functions. Her tenure at QuintilesIMS was marked by her leadership in global quality assurance, where she managed strategic alliances, developed enterprise-wide standard operating procedures, and drove continuous improvement initiatives that enhanced operational efficiency and customer satisfaction.
Liz’s passion for mentoring and leadership development extends beyond her corporate roles. She has been a sought-after speaker at numerous industry conferences, addressing topics related to quality assurance, healthcare compliance, and regulatory best practices. Her ability to translate complex regulatory requirements into actionable strategies has made her an invaluable resource for both emerging and established organizations. As a firm believer in fostering the next generation of industry leaders, she actively engages in mentorship, coaching professionals to navigate the evolving landscape of compliance and quality management.
Her influence extends globally, having worked across international markets to establish and maintain quality and compliance programs that meet the stringent expectations of regulatory bodies worldwide. She has served on various boards and committees, contributing her expertise to advance industry standards and best practices. Liz is an active member of the Society of Quality Assurance, the Association for Quality and Participation, and the Parenteral Drug Association. She has also been a member of the Maryland State Governor’s Quality Award Examiners Board, further solidifying her reputation as a leader committed to excellence in governance and compliance.
Beyond her professional achievements, Liz is deeply passionate about STEM advocacy, community service, and fostering leadership through mentorship. She believes in the transformative power of quality-driven organizations and the critical role that integrity, respect, and opportunity play in shaping corporate success. Her personal mission statement, “Truth, Respect, Opportunities, Love, and Laughter,” encapsulates the values she brings to every endeavor, both professionally and personally.
As she seeks new board opportunities, Liz aims to leverage her extensive experience in pharmaceutical development, quality assurance, and regulatory compliance to support organizations in their pursuit of excellence. With a proven track record of leadership, strategic problem-solving, and the ability to foster cross-functional collaboration, she is well-positioned to provide valuable insights and guidance at the highest levels of governance. Whether advising on quality strategies, mentoring future executives, or driving initiatives that enhance regulatory compliance, Liz remains committed to making a meaningful impact in the industries she serves.
Character: Elizabeth M. Troll is a principled leader who upholds integrity, respect, and mentorship as core values in fostering a culture of excellence and accountability.
Knowledge: With over 42 years of expertise in quality assurance, regulatory compliance, and governance, she possesses deep industry knowledge spanning pharmaceuticals, biopharmaceuticals, and healthcare.
Strategic: Liz excels in developing and implementing global quality management systems and compliance frameworks that align regulatory requirements with business objectives to drive operational success.
Communication: A skilled speaker and mentor, she effectively translates complex regulatory concepts into actionable strategies, fostering collaboration across teams and organizations.
