Liisa Eisenlohr is an Associate Director at Guidehouse within the Healthcare and Life Sciences Disputes, Regulatory, Compliance and Investigations practice, bringing more than 20 years of experience within the life sciences industry. Liisa has spent the past ten years in various global roles in medical affairs and clinical development at biopharmaceutical companies in the San Francisco Bay Area with a focus on bringing oncology drugs to market.
Prior to this, she worked in the tissue banking/medical device and bioreagents industries where she established and managed marketing, client services, and distribution departments. Liisa’s broad skill set includes experience in various areas of medical affairs, regulatory affairs, compliance, health economics and outcomes research (HEOR), and clinical trial management. She has supported such projects as effective global clinical trial initiation and ongoing monitoring; creation of technical documents for regulatory submissions; and establishing post-marketing adverse event reporting systems.
PhD, Molecular Biology/Biochemistry, Ruprecht-Karls-Universität, Heidelberg, Germany Master of Biological Sciences, Ruprecht-Karls-Universität, Heidelberg, Germany Master of Business Administration, The College of William & Mary, Raymond A. Mason School of Business
CCRA, Association of Clinical Research Professionals (ACRP) Certificate, Health Economics and Outcomes Research, University of Washington Graduate Certificate, Pharmaceutical and Medical Device Law and Compliance, Seton Hall University School of Law,