SANTA BARBARA, CA--(Marketwired - Feb 5, 2014) - USDM Life Sciences, a leading global regulatory consulting firm in the life sciences industry, is proud to announce Kathleen Warner, PhD is now Vice President of the Project and Program Management Practice.
Warner will use her Life Sciences management background to help USDM Life Sciences expand their project and program management services. Warner has over 25 years of experience as a professional manager, executive, trusted advisor and thought leader in Information Technology (IT) and Life Sciences. Over the years, Kathleen has managed large, complex, global organizations in a matrix environment.
Over the past 12 years, Warner's career expanded into Life Sciences where she held a variety of positions, including R&D Practice Head, PMO Executive, Business Development Executive, Consulting Partner and LS Domain Expert to name just a few. Kathleen has worked as a practitioner and futurist with many of the top pharmaceutical, medical device and biotechnology multinationals and has built organizations to successfully manage people, projects and programs.
USDM Life Sciences is committed to deliver project and program management excellence to its clients. With Kathleen's leadership and expertise in building the Project and Program Management Practice, USDM is well positioned to provide services that utilize technology for planning, managing, risk mitigation, feedback and accountability, all of which are crucial for successful project delivery, continued growth and client delight.
"Kathleen is a seasoned veteran in the Life Sciences industry with a solid track record of forward thinking and delivering results," said Kevin Brown, Managing Partner, USDM Life Sciences. "Our team is committed to continued excellence and growth. We believe Kathleen's experience will position us for growth and enhance our already strong council of practice leaders."
Warner holds a PhD in Education and Technology and is a certified Project Manager.
About USDM Life Sciences:
USDM Life Sciences is a leading global regulatory consulting firm providing compliance, validation, qualification, quality, auditing and information technology services via project teams and staff augmentation to our clients in the medical device, biotechnology, biologics, diagnostics and pharmaceutical industries. USDM Life Sciences has more than 13 years of experience supplying our clients in the life science industry with compliance services during each phase of their drug and product development cycle while partnering with best of breed organizations to help companies simplify, unify and optimize their business and compliance objectives. For more information, please visit www.usdm.com.