An experienced Biopharma Executive with over 25+ years’ experience Greg has developed and successfully executed financially responsible strategies in executive level roles ranging from CEO, COO, Sales Management, Market Access, Marketing, and Business Development.

Greg has consistently demonstrated the ability to build and effectively manage departments across a myriad of therapeutic classes.  Most recently at Zimmer Biomet/Biologics Division as VP, Marketing, Greg managed and developed successful strategies for the companies first prescription injectable product, Gel-One.  While at Savient Greg lead the build out of the company’s biologics arm taking responsibility for Operations, Sales and Managed Care in support of Euflexxa the company’s first biologic launch.

Recruited by Andrx Laboratories, he was part of the senior management team that established Andrx in the branded marketplace and took responsibility for managing the team that successfully launched Altoprev and Fortamet the company’s first branded products. Beginning his career at Forest Laboratories Greg quickly elevated himself and took responsibility for the Managed Care department in support of the company’s first blockbuster Tiazac.

Greg is an industry consultant for Gerson Lehrman Group, Third Bridge and an associate member of the Academy of Managed Care Pharmacy.

Greg graduated from Illinois State University with a degree in Political Science.

Dr. Spellman is a board-certified dermatologist with a long history of diverse roles in the biopharmaceutical industry supporting the development of topical, systemic, and biological therapeutics for dermatologic, immunologic, and oncologic indications from discovery through commercialization.

Prior to joining Castle Creek, Dr. Spellman managed the planning and execution of clinical programs as Chief Medical Officer of Menlo Therapeutics. She previously provided executive level consulting services as a medical and safety officer, and as a development strategist, to multiple biopharmaceutical and device companies. Prior to establishing her consulting business, Dr. Spellman held medial leadership positions at Revance Therapeutics, Biogen Idec, Connetics Corporation, and Novartis Pharmaceuticals, primarily supporting the development of novel dermatologic and immunologic therapies. Dr. Spellman has been instrumental in achieving US FDA and ex-US approvals for multiple topical and systemic therapies.

Until 1997, Dr. Spellman sustained an academic clinical practice, directing the Residency Training Program and the Clinical Research group in Dermatology at the University of California, San Diego. Dr. Spellman earned her M.D. from the Medical College of Wisconsin, and is a diplomate of the American Board of Dermatology and a fellow of the American Academy of Dermatology.

Ron brings more than 30 years’ experience in the pharmaceutical industry.  Ron is an accomplished operations executive with a broad experience base in drug development, clinical and commercial manufacture of biologics. Ron also has an in depth experience in aseptic processing and manufacturing parenterals.

Ron’s career started at Johnson & Johnson where he held several leadership roles and ultimately was responsible for a worldwide launch of a new blood type and screening diagnostic.  Ultimately Ron became responsible for Johnson & Johnson’s Blood Bank Operations, which included their parenteral vaccine division.

Due to Ron’s broad based background he has been key in transitioning small to mid-sized biopharmaceuticals from R & D to commercial manufacturing to accomplish successful launch. In addition to Johnson & Johnson, Ron also held several leadership roles at Liposome, Elan, Enzon, NPS and Shire Pharmaceuticals.   Ron has worked on a wide range of products that encompass unique processes such as liposomal encapsulation, PEGylation, lypohilization, plasma fractionation, etc.  His responsibilities have not only encompassed domestic responsibilities, but he has been responsible for CMO oversight and worked international throughout Europe and Asia.

In virtually every role, Ron has been responsible to ensure compliance with respect to cGMPs and has a vast amount of experience working with regulatory agencies such as the FDA and EMEA.  He has been key in reviewing and writing INDs, NDAs, SNDAs, MBRs, SOPs, RFPs, SOWs and has been instrumental to ensure readiness for PAIs.

Ron also has an extensive background in Project Management, which has encompassed technology transfer, scale-up and build-out of sterile manufacturing facilities.

Ron holds a BS degree in biology from Rutgers University and an M.B.A. in Business from Fairleigh Dickinson University.