Kevin Barber, MS, PhD, RAC, PMP is Vice President of Regulatory Affairs and leads the development and execution of Novan’s regulatory strategy. Dr. Barber has over 21 years of experience in pharmaceutical product development and biomedical research with a background in designing and implementing effective integrated regulatory plans. Most recently, Dr. Barber served as Vice President of Global Brand Regulatory Affairs at Actavis (formerly Watson Pharmaceuticals) where he was responsible for regulatory development of over 20 products and regulatory life cycle management of more than 150 approved products in US, Canadian, and European markets.
Carri Geer, Ph.D., is the Vice President of Pharmaceutical Development and leads the drug substance, drug product, device and analytical development for Novan’s drug candidates. Additionally, Dr. Geer serves as the technical liaison for collaborative partnerships. Dr. Geer has approximately 10 years of experience in pharmaceutical product development with a background in analytical and bioanalytical chemistry. During her tenure at Novan, Dr. Geer has been responsible for establishing and growing the analytical capabilities of the Company. Prior to joining Novan, Dr. Geer was employed at Merck and bridged the interface between R&D and cGMP analytical testing.
Stan Hollenbach, BS, JD, is the Senior Vice President of Research and Development and leads all phases of pharmaceutical drug development other than clinical testing of Novan’s product candidates. Mr. Hollenbach has more than 25 years of experience in the biotechnology industry specializing in preclinical development of small molecules and proteins which included participation in numerous US and European regulatory submissions. Prior to joining Novan in 2014, Mr. Hollenbach was the vice president of pharmacology at Portola Pharmaceuticals, Inc., where he focused primarily on platelet and fibrin mediated thrombosis, leading the preclinical development of orally bioavailable antiplatelet P2Y12 antagonists and the factor Xa inhibitors andexanet alpha and betrixaban. He also worked previously at COR Therapeutics which was acquired by Millennium Pharmaceuticals and Genetech as well as served in the US Army at the Letterman Army Institute of Research (LAIR) with research experience in emergency care and resuscitative therapy of combat casualties.
Jeff N. Hunter, MS, is the EVP and Chief Business Officer and has been integral to the company’s execution and operational success since its inception. With more than 35 years of broad business experience including as co-founder and former CEO and Chairman of a small-cap public company, Mr. Hunter has built Novan’s manufacturing and corporate infrastructure as well as strengthened supply chain and business relationships. His versatility and in-depth understanding of the company’s business includes the role of corporate secretary. In 2013, the Triangle Business Journal recognized Mr. Hunter as a top executive in his field. In 2015, he was appointed to serve on the Board of Directors of the North Carolina Biotechnology Center.
Tomoko Maeda-Chubachi, MD, PhD, MBA, is the Vice President of Medical Dermatology and provides medical input to help drive the strategy, design and execution of Novan's development programs. Most recently, she served as senior medical director at GSK, leading clinical development projects for psoriasis, atopic dermatitis, pemphigus and androgenic alopecia. Prior to GSK, she held clinical and medical affairs roles at Eli Lilly and Company and Pfizer, Inc. Dr. Maeda-Chubachi was an academic physician and dermatologist for ten years before entering the pharmaceutical industry.
G. Kelly Martin is interim Chief Executive Officer of Novan, Inc. He served as CEO of Elan, Ireland’s largest indigenous biotech company, from February 2003 until its successful $8.6 Billion sale to Perrigo Company in December 2013. Before joining Elan, Mr. Martin spent more than 20 years at Merrill Lynch & Co., Inc., where he held a broad array of operating and executive responsibilities. Mr. Martin also serves as a non-executive director on a number of public and private company boards and is a co-founder and director of Brandon Point Industries.
Tim O’Sullivan, JD, MBA, is the Vice President of Intellectual Capital and spearheads the strategic development of Novan’s intellectual property portfolio. He manages Novan’s licensing strategy and is responsible for building the Company’s robust barriers to entry. Mr. O’Sullivan has more than 20 years of experience in developing intellectual property portfolios. Before joining Novan, Mr. O’Sullivan was the director of intellectual property and business development for LED Lighting Solutions at Cree, Inc.
Paula Brown Stafford, MPH, is the Chief Development Officer and leads the tactical execution of clinical trials and the establishment of statistics and data management functions for Novan. Prior to joining Novan, she served as president of clinical development at Quintiles (now QuintilesIMS), where she was responsible for all Phase I-IV clinical development operations globally, reaching $3 billion in annual revenue. In addition to her role at Novan, Ms. Stafford continues to participate in other professional activities, including serving as a director at Health Decisions, Inc. and adjunct professor in Public Health Leadership at the Gillings School of Global Public Health at The University of North Carolina at Chapel Hill, and also maintains her third-party consulting business. She was named as one of the 10 top women in biotech by FierceBiotech in 2012, recognized as a Distinguished Alumna at UNC Chapel Hill in 2016, and recently designated an NACD Governance Fellow. She holds a Bachelor of Science and a Masters in Public Health, both from The University of North Carolina at Chapel Hill, with her specialization in Biostatistics.
Nathan Stasko, PhD, is co-founder, President and Chief Scientific Officer and a Director of Novan, Inc. Dr. Stasko has led the transformation of the Company’s nitric oxide platform from the academic benchtop to Phase 3 clinical trials and is considered a leading expert in the field of nitric oxide. He is an inventor of the core Novan technology and of more than 100 patent filings, 19 of which have issued, and has authored several peer-reviewed manuscripts pertaining to the chemical storage and controlled release of nitric oxide. Dr. Stasko has led the Company through each of its private financings totaling more than $100 million, as well as the award of government grants and contracts totaling $15 million, the latter ultimately resulting in Novan’s national recognition as a Tibbetts Award winner for excellence in Small Business Innovation Research. He has assembled a team of highly experienced executives and skilled professionals with drug development and commercialization expertise, who share his vision to position Novan as a commercially successful leader in the dermatology market.