About Me


Hello! I'm Liisa Eisenlohr.

With over 25 years of experience in global and country-level roles in the pharmaceutical/biotechnology industry and in Life Sciences consulting, I have the experience to provide strategic and project-based leadership as well as short-term operational/staffing support for Medical Affairs and Healthcare Compliance functions in start-up, mid-sized, and established corporations. With both German and American citizenships, I am fluent in German and English.

As an engaged and self-motivated independent consultant with an enthusiastic approach and the ability to lead and motivate others to achieve corporate goals, I have a proven record of successfully establishing and growing new departments in start-up and growth organizations. I am able to work independently as well as a committed team member to ensure timely delivery of results on complex projects. I possess sound knowledge of ICH/GCP guidelines and relevant U.S. FDA and European regulations.

Brief Curriculum Vitae

Owner and Senior Advisor – Medical Affairs, Healthcare Compliance, and Clinical Development • ArteMedIQ August 2022 – Present

Associate Director • Guidehouse (previously Navigant Consulting) April 2017 – July 2022

Applied expertise acquired in the Life Sciences industry to assist clients with overcoming their organizational challenges, including:

• Advising on global Medical Affairs activities, including medical engagement and operating model design; compliant scientific/medical communications with healthcare professionals; publication planning, strategy, and execution; advisory board management; review of promotional and non-promotional materials; medical information strategy and document development; educational grant management; and investigator-initiated and non-interventional study oversight both pre-and post-product launch

• Collaborating closely with clinical and commercial functions to support development of communication and business plans for medical product launch preparation and readiness

• Establishing comprehensive compliance and risk assessment programs and auditing and monitoring programs for life science companies of varying sizes; developing policies and standard operating procedures (SOPs) for Medical Affairs function

Senior Director, Global Medical Information • Clovis Oncology July 2015 – March 2017

Led Global Medical Information and US Pharmacoeconomics/Health Outcomes functions for all products, ensuring timely, high-quality responses to inquiries from healthcare providers around the world, and developing and providing scientific/medical training on the company’s products as well as non-small cell lung and ovarian cancer.

Director, Scientific Communications • Medivation February 2013 – June 2015

Led scientific/medical communication activities, including medical information, independent medical education, and peer-reviewed publications (congress posters and presentations; medical journal articles). Collaborated with medical field staff and other internal stakeholders to ensure continuous and timely training on scientific aspects of the company’s products as well as prostate cancer and breast cancer.

Clinical Scientist (trastuzumab emtansine/T-DM1) • Genentech January 2012 – January 2013

Senior Global Publications Leader, Oncology • Genentech/Roche June 2008 – January 2012

Director, Physician and Medical Staff Education • LifeNet Health September 2001 – May 2008

Director, Client Development and Support • ActiveCyte January 2001 – August 2001

Manager, Marketing Communications • Cell Signaling Technology October 1999 – December 2000

Director, Client Relations • Upstate Biotechnology June 1995 – September 1999

Education and Training


Master of Business Administration (MBA) • The College of William and Mary, Raymond A. Mason School of Business, USA 2001 – 2004

Dr. rer. nat., Biochemistry and Molecular Biology • Ruprecht-Karls-Universität Heidelberg, Germany 1983 – 1995


Board Certified Medical Affairs Specialist (BCMAS) from the Accreditation Council for Medical Affairs (ACMA)

Certified Compliance & Ethics Professional–International (CCEP-I) from the Society of Corporate Compliance and Ethics (SCCE)

Certified Clinical Research Associate (CCRA) from the Association of Clinical Research Professionals (ACRP)

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