Mr. Schelling has 20 years of commercial strategy and orphan drug development expertise. Prior to founding Acer, he was Executive Director of Strategic Marketing at BioMarin Pharmaceutical (BMRN), where he was instrumental in the development and commercialization of the company’s phenylketonuria (PKU) franchise. Previously, he held roles at Abgenix, Cell Therapeutics, SRI Consulting, and Organon. He is currently also a Director and Founder of Censa Pharmaceuticals Inc. and a Director of Cascade Prodrug, Inc.
Mr. Palmin has 25 years of corporate experience. He spent 15 years at Novelos Therapeutics (NVLT), where he served as President and CEO and Board Director and built the company from concept to a $500M peak market cap; raised $98 million in funding; and oversaw ten clinical studies in oncology (including pivotal Phase 3 studies) and infectious diseases. Previously, he held roles at Lehman Brothers and Morgan Stanley.
Dr. Will Andrews joined Acer Therapeutics as Chief Medical Officer in October of 2017. He has worked in the biotech/pharmaceutical industry for 17 years in both Clinical Development and Medical Affairs, and has worked in multiple therapeutic areas, with a focus and extensive experience in rare diseases. Dr. Andrews has significant medical marketplace and product launch experience, having served as the medical lead for six product launches, including Xopenex HFA®, Brovana®, Alvesco®, Omnaris®, Catena®, and Juxtapid®. Most recently, he provided strategic consulting services to rare disease companies in Clinical Development, Medical Affairs, Go-To-Market/Launch planning, and Business Development/Corporate Strategy. Previously, Dr. Andrews held senior leadership positions and positions of increasing responsibility at Aegerion Pharmaceuticals, Santhera Pharmaceuticals, Sepracor, and ClinQuest. He received his undergraduate degree in Biology from Harvard University and his MD degree from Yale University School of Medicine. Dr. Andrews practiced medicine for 7 years full-time and 11 years part-time in the Boston area as a Board Certified Internist and an Attending Physician at Brigham and Women’s Hospital, and was on the Clinical Faculty at Harvard Medical School.
Don Joseph joined Acer as Chief Legal Officer and Secretary in April 2018. He has over 20 years of biopharmaceutical industry experience, including general counsel and senior management positions in biopharmaceutical and global health organizations. Mr. Joseph served as Chief Legal Officer and Board Secretary of KaloBios Pharmaceuticals, Inc., a publicly listed biopharmaceutical company. Prior to KaloBios, he was Chief Executive Officer, and before that, Chief Operating Officer of BIO Ventures for Global Health, or BVGH. Mr. Joseph is currently a member and Secretary of the BVGH board of directors, having served previously as its Chairman. He previously served as general counsel, corporate secretary, and in other senior management roles at publicly held biopharmaceutical companies, including Abgenix and Renovis. Mr. Joseph currently serves as lead independent director of Achieve Life Sciences, a publicly held pharmaceutical company. Before entering the life sciences industry, he practiced corporate law for a number of years in major firms, including as an international partner at Baker & McKenzie, one of the world’s largest law firms. Mr. Joseph received his J.D. degree from the University of Texas School of Law, with honors.
Ms. Pound joined Acer as Vice President, Marketing in April 2019. She brings over 25 years of biotech and pharmaceutical experience with expertise in marketing and commercial leadership. During her career, Ms. Pound has worked in multiple therapeutic areas including neurology, rare diseases, immunology, respiratory and pain. Prior to joining Acer, she was the Senior Director, Marketing for Neurocrine Biosciences where she was the commercial lead for a phase III molecule for Parkinson’s Disease. Previously, Ms. Pound held roles of increasing responsibilities with companies such as Avanir, Questcor, UCB and Dey, L.P. She has significant marketing and launch experience having worked on products such as Neudexta, Acthar, Cimzia and EpiPen. Ms. Pound received her degree in Marketing from The University of Missouri.
Mr. Paul’s has over 25 years of experience in human resources. He most recently served as vice president of human resources at Clarisonic, a device company acquired by L’Oreal. Over his career he has played a major role in developing organizational cultures within various companies assisting them in scaling through different stages of growth while achieving significant milestones including IPO’s, M&A integrations and product commercialization. Mr. Paul has held senior HR leadership roles at Trubion Pharmaceuticals (acquired by Emergent BioSolutions) and Corixa Corporation (acquired by GSK). He holds a B.S. from MSU-Billings and an M.S. from SUNY Buffalo State.
Mr. Seibt joined Acer as Vice President, Market Access and Reimbursement in April 2018 and was promoted to Interim Head of Commercial in March 2019. He has over 22 years of health care industry experience in sales and leadership with 15 years of specialization in managed care market access and reimbursement. During his career, Mr. Seibt has successfully launched 19 products in primary care, specialty and rare diseases. Prior to joining Acer, he was the Director of Account Management, where he led a field market access team dedicated to securing distribution, formulary coverage and reimbursement of Biogen’s portfolio in hemophilia, multiple sclerosis and spinal muscular atrophy. Previously, Mr. Seibt held roles in sales, marketing and market access at Pfizer, Vertex, PCA HealthPlans and PacifiCare. He received his degree in economics at The University of Texas and completed the healthcare leadership program at Portland State University.
Mr. Robinson joined Acer as Vice President, Information Technology in September 2018. He has over 20 years of information technology experience with expertise ranging from business transformation to cloud to strategic sourcing. Prior to joining Acer, Mr. Robinson was a Director at Apps Associates where during his tenure he operationalized two strategic offerings (Oracle EBS R12 migration and Application Managed Services) with responsibilities that spanned business development, financial management and operations. Prior to Apps Associates, he has held roles spanning business analysis through project management in technology companies such as Oracle, CSC, Akamai, and Siemens. Mr. Robinson earned his B.S. degree in Accounting from Boston College and his M.S. degree in Information Technology from Bentley University.
Ms. Mulready joined Acer as Vice President, Program and Alliance Management in April 2018. She has over 20 years of biotechnology experience with expertise in executional strategy and team leadership. Prior to joining Acer, Ms. Mulready was Senior Director of Program and Alliance Management at Mersana Therapeutics where she launched the function with responsibility for establishing and leading governance and teams, driving the business processes to advance the multiple internal and partnered programs, and ensuring efficiency in delivering on goals across the portfolio. Previously, she held roles of increasing responsibility at ImmunoGen, Inc. spanning Program Management, Alliance Management and Discovery Research. Ms. Mulready earned her B.A. degree in Biology from Colby-Sawyer College and her M.S. degree in Management from Lasell College.
Ms. Lonnroth joined Acer as Vice President, Quality starting in May 2018. She brings more than 20 years of experience implementing, improving and directing Quality initiatives in highly regulated global life science corporations. Ms. Lonnroth is a subject matter expert in Quality Assurance (QA) / Quality Control (QC) and Quality Management Systems (QMS) and has successfully hosted several FDA and other agency inspections and customer/partner audits. Prior to Acer, she has held leadership positions in Commercial and Pre-Commercial Quality at several companies including AMAG Pharmaceuticals, Celestica, Acusphere, Histogenics, Stryker Biotech and Alkermes. Ms. Lonnroth obtained her US Regulatory Affairs Certification (RAC[US]) from RAPS in 2011. She received her B.A. degree in Modern Languages and B.S./M.S. degrees in Chemistry at University of Massachusetts, Lowell and her MBA at Franklin Pierce University.
Mr. Kneeland joined Acer as VP Finance, Controller in November 2017. He brings over 20 years of progressive experience in the corporate finance leadership of technology and related companies. Prior to joining Acer, Mr. Kneeland was VP Finance at TechTarget, Inc., a public company with 700 employees and $100M of annual revenue, where he led a team responsible for the day-to-day finance and accounting operations, as well as several key initiatives around revenue recognition and systems implementations. Prior to TechTarget, Mr. Kneeland was a Senior Manager at CFGI, where he assisted domestic and international bio-tech and technology clients with public offerings, mergers and acquisitions and other complex accounting, reporting and internal-control matters. Prior to that, Mr. Kneeland was Director of Technical Accounting of a multi-billion-dollar publicly traded retail pharmacy and pharmacy benefit management company. He has fulfilled various accounting and reporting roles with publicly traded companies in the technology industry since beginning his career in the audit practice of KPMG LLP. Mr. Kneeland is a Certified Public Accountant in the state of Massachusetts and holds a Bachelor of Science in Accounting from Johnson & Wales University.
Mr. Klopp joined Acer as Vice President, Manufacturing in January 2018. He brings over 18 years of experience in the biopharmaceutical industry developing small molecule drug candidates in positions ranging from research to process development to contract manufacturing management. Mr. Klopp has spent the last 11 years working on the development and commercialization of orphan drugs at BioMarin Pharmaceutical (BMRN) and later Ultragenyx Pharmaceutical (RARE). His expertise includes selecting and managing contract manufacturing sites producing drug substance and various oral dosage forms including associated sponsor clinical and commercial CMC regulatory strategy. Mr. Klopp received a B.S. degree in Chemistry from Pennsylvania State University and a M.S. degree in Chemistry from University of California at Berkeley.