ThinkLive 2025 CGT Summit

Speakers

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Ann-Sophie Kuschel 

Principal Consultant, Vintura

Ann-Sophie Kuschel is a Principal with over nine years of experience in strategy consulting, specializing in support for pharmaceutical, MedTech, and biotech companies. She possesses a strong background in various market access activities and is a core member of the Cencora EU HTA Center of Excellence. Ann-Sophie focuses on market access, clinical trial, and value communication projects. She is trained as a pharmacist and holds a PhD in Pharmaceutical Sciences from the University of Tübingen in Germany.

Arvind Natarajan, PhD, MBA

Senior Vice President of Process and Analytical Development, Iovance Biotherapeutics

Arvind Natarajan, PhD, MBA, is Senior Vice President of Process and Analytical Development at Iovance Biotherapeutics, where he has worked on development and commercialization of AMTAGVI™ (lifileucel), the first approved T cell therapy for solid tumor cancer. He has 25 years of CMC experience in cell and gene therapies, biologics, and vaccines.

Prior to joining Iovance, Dr. Natarajan was Global Head of Program Management and Strategy, Cell & Gene Technical Development and Manufacturing at Novartis. Prior to that, he was the Global CMC Lead for Kymriah®, the first FDA-approved CAR-T therapy.

Prior to joining Iovance, Dr. Natarajan was Global Head of Program Management and Strategy, Cell & Gene Technical Development and Manufacturing at Novartis. Prior to that, he was the Global CMC Lead for Kymriah®, the first FDA-approved CAR-T therapy.

Prior to Novartis, Dr. Natarajan worked at Merck and Co for 15 years. While at Merck, he worked in biologics on tech transfer and approval of Keytruda®, and in vaccines, supporting development, approval, and commercial manufacturing of Zostavax®, ProQuad®, and Varivax®.

Dr. Natarajan earned an MBA from Wharton, a PhD in Chemical Engineering from University of Minnesota, a Masters in Microbial Engineering from University of Minnesota, and a Masters in Biology and BE in Electronics and Electrical Engineering from Birla Institute of Technology and Science (BITS), Pilani in India.  

Ashley Dalton

Associate Chief Pharmacy Officer for Ambulatory Infusion, UC San Diego Health

Dr. Dalton is the Associate Chief Pharmacy Officer for Ambulatory Infusion at UC San Diego Health, where she has served in various roles since 2005. She earned her Doctor of Pharmacy degree from the University of Kansas and completed acute care residency training at UC San Diego Health. Additionally, she completed training with the ASHP Foundation Pharmacy Leadership Academy and earned a Masters in Healthcare Administration from Simmons College.  Dr. Dalton is an active leader in professional organizations, serving on the NCCN Products and Services Committee and as a representative for UC San Diego Health on the NCCN Pharmacy Directors Forum. She is also a member of the Vizient Pharmacy Business Council and BD Thought Leader Committee. Previously, she contributed to the Novation Taskforce for Automation, and the Vizient Pharmacy Network Cancer Care Committee.  Her contributions have been recognized with the Vizient Pharmacy Vision Award for Jon Kim Excellence in Strategic Sourcing (2023) and the University of California Loss Prevention Grant (2020).  Passionate about advancing pharmacy practice, Dr. Dalton is dedicated to driving safe, effective, equitable, and cost-conscious healthcare solutions. With an infectious enthusiasm for pharmacy, she leverages her positive attitude and tireless work ethic to inspire and empower others toward success.

Ben Shaffer, RPH, MBA

Senior Director, Cell & Gene Therapy Enterprise 

Ben Shaffer serves as the Senior Director, Cell & Gene Therapy Enterprise Business Partnerships for Biopharma Services at Cencora. In his role, Ben is responsible for working closely with Cell & Gene manufacturers and clinical trial sites to ensure they have knowledge, insight and access to Cencora’s comprehensive end-to-end clinical trial and commercialization support services.

Ben has been with Cencora for over 12 years and has held various roles prior to joining the Cell and Gene team.  Most recently, Ben served as the National Vice President of Distribution Business Development and Client Strategies for the U.S. market.   Before this role, he spent over 7 years providing consultative solution sales supporting Cencora’s 75 largest Integrated Delivery Networks across the U.S.  

Before joining Cencora, Ben spent over 14 years in various Health System leadership roles, including Pharmacy operations and Business Development, both as a Director of Pharmacy and also as a Director of Business Development leading ambulatory expansion for Oncology, Neurology, Urgent and Primary care services.

Ben received his Bachelor of Pharmacy degree from Ohio Northern University, and his Master of Business Administration in Healthcare from Columbia Southern University. 

 

Christian K Schneider, M.D.

Vice President & Chief Medical Officer, Clinical Development Services, Cencora PharmaLex

Christian K Schneider, M.D., is Vice President & Chief Medical Officer, Clinical Development Services,  at Cencora PharmaLex. Before joining PharmaLex, Christian was interim Chief Scientific Officer at the UK’s medical products regulator, the Medicines and Healthcare products Regulatory Agency (MHRA), and Director of the National Institute for Biological Standards and Control (NIBSC), a Center within the MHRA. Christian has broad global regulatory authority experience, having served as Medical Head of Division Medicines Licensing & Availability at the Danish Medicines Agency and as Head of Division EU Cooperation/Microbiology at the Paul-Ehrlich-Institut, Germany’s Federal Agency for Vaccines and Biomedicines. Christian was co-opted member of the Committee for Medicinal Products for Human Use (CHMP) at the European Medicines Agency (EMA), Chair of EMA’s Committee for Advanced Therapies (CAT), Chair of EMA’s Biosimilar Medicinal Products Working Party (BMWP), and member of EMA’s Scientific Advice Working Party (SAWP). As a regulatory scientist, he has published more than 50 articles in international peer-reviewed journals. 


Darin DeCarlo

Chief Commercial Officer, Orsini

Darin DeCarlo is the Chief Commercial Officer for Orsini, a leading national specialty pharmacy focused on rare disease and cell and gene therapy.  In this role his responsibilities include business development, marketing, commercial operations, and sales. Darin has over 35 years of industry experience spanning both big and small pharma, consulting, and specialty pharmacy.  

His 26 years in pharma and biotech experience include about 20 years between Eli Lilly and Roche in various commercial leadership roles mostly in sales and marketing. Most recently he served as Vice President of Sales and Managed Markets at Acadia Pharmaceuticals.  Darin also spent five years at IQVIA, primarily leading launch and commercial consulting before joining Orsini in 2022. 


David L. Sokoloff

Executive Director of Supply Chain, Precigen, Inc. 

Originally from New Jersey, David’s academic career includes a B.A. from Gettysburg College in Economics, a M.A. in International Development Studies from the Elliott School at George Washington University, and an MASc in Supply Chain Management from Massachusetts Institute of Technology. David began his professional career in manufacturing and finance before serving with the U.S. Peace Corps in the Republic of Kiribati. Since, he has spent over 20 years on humanitarian focused initiatives.

In 2006, David founded For Granted, Inc., a 501(C)(3) nonprofit committed to improving lives in underserved communities. Over the past 30 years, For Granted has supported programming in education, water and sanitation, micro-finance, and child health around the world.

David has managed supply chains for emergency efforts throughout Europe, Africa, Asia, and the Middle East. He ran operations with Doctors Without Borders prior to working in Washington, D.C. leading global logistics operations.

At the onset of the COVID outbreak, David joined Novavax and led supply chain operations delivering vaccines throughout the world. David currently leads the Supply Chain program at Precigen, Inc.

Precigen is a dedicated biopharmaceutical company advancing the next generation of gene and cell therapies using precision technology to target the most urgent and intractable diseases in immuno-oncology, autoimmune disorders, and infectious diseases. The commercial launch of PRGN-2012, for the treatment of adults with recurrent respiratory papillomatosis, is anticipated later this year.

David and his wife currently live in Washington, D.C. with their three children. 

Dawn Ratfelders 

Senior Director of Patient Services and Field Reimbursement, Neurotech

Dawn Ratfelders is a seasoned pharmaceutical and biotechnology professional with over 25 years of experience across patient services, market access, distribution, and marketing within rare disease and specialty therapeutic conditions. She currently serves as Senior Director of Patient Services and Field Reimbursement at Neurotech, where she is responsible for building and leading the organization’s patient services and reimbursement infrastructure to support the successful commercialization of Neurotech’s encapsulated cell-based gene therapy.

Elizabeth Turcotte 

Vice President and Head, Patient Affairs, Pierre Fabre Pharmaceuticals

As a core member of Pierre Fabre Pharmaceuticals executive team, Elizabeth Turcotte leads the development and execution of US patient strategy and serves as an enterprise-wide steward of the patient experience. She champions and oversees all strategic and operational aspects of patient engagement across advocacy, access, and education as well as culture and corporate communications.

Throughout her career, Elizabeth has been dedicated to enhancing the patient and customer experience. Her philosophy and approach are rooted in co-creating patient-centric services, programs, and educational resources alongside patients, caregivers, advocacy organizations, and healthcare providers. This ensures that patients' voices are heard, and their needs effectively addressed.

Before joining Pierre Fabre Pharmaceuticals, Elizabeth served as Executive Director, Head of Patient Experience at Kite Pharma, where she successfully led the development and execution of an organization-wide patient experience strategy. Prior to that, she held leadership roles at Cisco and Bristol Myers Squibb, where she established the enterprise-level patient experience function and spearheaded the development of Universal Patient Language.

Elizabeth holds a BA in Economics from Binghamton University and an MBA from William & Mary School of Business. Outside of work, Elizabeth enjoys traveling and antiquing with her husband.

Elizabeth holds a BA in Economics from Binghamton University and an MBA from William & Mary School of Business. Outside of work, Elizabeth enjoys traveling and antiquing with her husband. 

Eric Schier 

Senior Manager of Personalized Supply Chain, Cencora World Courier

Eric Schier serves as the Senior Manager of Personalized Supply Chain for Cencora World Courier. In his role, Eric is responsible for leading the design and development of solutions for the CGT and DTP service lines for both clinical and commercial commodities. Ensuring that the VOC (Voice of the Client) is well understood through the multiple internal channels that Eric liaises with on a daily basis.

Eric brings a unique perspective from his 20+ years in biotech, pharma, CGT space working for sponsors, CDMOs, and specialty logistics providers seeing the need and solution from every angle. Most recently, Eric served as a Senior Manager in the supply chain at Bristol Myers Squibb CGT division. 

George Eastwood

Executive Director, The Emily Whitehead Foundation

George Eastwood currently serves as Executive Director for The Emily Whitehead Foundation. Emily is widely known as the first pediatric CAR-T patient and the Whitehead family created the foundation to ensure that more families could have the same outcome as theirs. Since its inception in 2015 the focus has been on funding groundbreaking research to create less-toxic treatments for pediatric cancer patients, while simultaneously advocating for increased access to these therapies and supporting patients on their treatment journey. George’s professional background has largely been focused on the creation of products, tools, and services that support the development of cell-based therapeutics. As an early employee at HemaCare he led global sales and business development, working to partner with developers to create cellular solutions to advance the development of autologous and allogeneic CAR-T cell therapies. He also has experience in the start-up space both at Kytopen where he served as VP of Business Development and Partnerships and at Excellos, where he was a co-founder and helped to spin out the company from the San Diego Blood Bank. In addition to his current role at The Emily Whitehead Foundation, George also sits on the advisory board of Truetrials.org, is a board member at CGT digitization company Autolomous, and is a board member for the Alliance for Regenerative Medicine. 

Guillaume Nebout

VP International Commercial Services, Cencora

Guillaume is qualified as a Pharm D and has two master degree in biologic sciences and biostatistics as well as an Executive MBA from leadings European Business Schools. He spent 4 years as a resident in the Parisian hospitals and afterwards joined the pharmaceutical industry. He started in clinical research and rapidly moved to evolving senior positions in international strategic marketing and local sales for 12 years.

Guillaume joined Walgreens Boots Alliance and moved to the UK in 2012, to lead the development of professional services through digital, medical and pharmaceutical services. He led a series of cross divisional work streams on innovations identification and deployment as well as influencing activities on the pharmacy regulatory environment both at the country and international level. Guillaume was also member of the Healthcare Innovation Platform, the cross-divisional team developing digital innovation for healthcare within WBA.

After this role, Guillaume was in charge of the strategic partnerships with the pharmaceutical industry (branded) for Europe to strengthen the synergies and ensure an efficient launch of their drugs.

Guillaume is now VP of International Commercialization Services and leads the operationalisation of global specialty launches within the International Commercialisation team, develops the company offers by opening new services and coordinates regional and local business teams.

Guillaume is an lifelong elected member of the French National Academy of Pharmacy.

Herbert Altmann

Herbert Altmann​

Vice President, Market Access and Healthcare Consulting Europe, Cencora

Herbert Altmann
Herbert Altmann, Ph.D., is Vice President, Market Access and Healthcare Consulting Europe at Cencora. He leads the European Market Access department, working with pharmaceutical companies bringing innovative medicines to patients with unmet medical need as fast as possible. Before joining Cencora, Herbert was Head Value & Access Region Europe Novartis Pharma, leading the Market Access department to ensure access for patients to Novartis brands. He was the NVS representative on the EFPIA HTA working group, participating in two Joint Action 3 assessments. 
Herbert Altmann

John Arena 

President, Global Pharma Services, Cencora

John Arena, President of Global Pharma Services, was previously in the role of Senior Vice President of Enterprise Strategy and Solutions and serves as the key executive contact for top global biopharma companies on behalf of Cencora. With a deep understanding of the challenges biopharma companies face, John and his team connect pharma partners to Cencora's broad range of experts and offerings to support product success and patient access worldwide.

Prior to joining Cencora, John held leadership roles at Lundbeck, Johnson & Johnson, and Eli Lilly & Company. His professional track record is marked by strong enterprise thinking and bold leadership across operations, marketing, sales, and new product planning.


Justin Konkol, Pharm.D., MHA, DPLA 

Executive Director of Pharmacy, Acute Care and Oncology Pharmacy Services, Froedtert & the Medical College of Wisconsin
Clinical Assistant Professor, Medical College of Wisconsin School of Pharmacy

Justin is a graduate of the University of Wisconsin, School of Pharmacy in 2006.  After graduation, he completed a Pharmacy Practice Residency (PGY-1) and Health-System Pharmacy Administration Residency (PGY-2) at Oregon Health and Science University (OHSU), in Portland, Oregon.  At the completion of his residency, he remained at OHSU through 2010 in a variety of pharmacy leadership positions.  Justin and his family relocated to Wisconsin in 2010 joining the staff at ProHealth Care in the greater Milwaukee area as a Pharmacy Manager.  Justin then joined the leadership team of Froedtert and the Medical College of Wisconsin Health system in 2012 and has held multiple leadership roles during his tenure, most recently being promoted to the Executive Director of Pharmacy, a role he has held since February of 2025.  Justin is a proud graduate of ASHP Foundation’s Pharmacy Leadership Academy (PLA) and received his Masters of Healthcare Administration from the University of Wisconsin-Milwaukee College of Health Sciences in 2020.  

Justin is an active member of several professional organizations including the Pharmacy Society of Wisconsin (PSW), American Society of Health-Systems Pharmacists (ASHP), American College of Healthcare Executives (ACHE) and Vizient’s Academic Pharmacy Network.  He serves as a clinical instructor for pharmacy students from several schools of pharmacy including the University of Wisconsin School of Pharmacy, Concordia University Wisconsin School of Pharmacy, and the Medical College of Wisconsin School of Pharmacy.  Justin also serves as the residency director for the PGY1/PGY2 Health System Pharmacy Administration and Leadership Residency at Froedtert Hospital.  

Justin’s professional interests include leadership development, lean management in health care, and pharmacy informatics and technology.  He lives in Sussex, Wisconsin with his wife Sarah, and his four children, James (15), Bridget (13), Sam (11), and Henry (8).  He is the oldest of five proud Konkol pharmacist brothers, all graduates of the University of Wisconsin, School of Pharmacy.  
 

Kevin Chinn

Vice President and Head of the Cell & Gene Therapy Service Line, Cencora

Kevin Chinn serves as Vice President and Head of the Cell & Gene Therapy Service Line for Cencora. In his role, Kevin is responsible for leading Cencora’s strategy to support cell and gene therapy developers in commercializing their innovative products. Kevin also leads the team responsible for developing strategic partnerships with cell and gene therapy companies. Under Kevin’s leadership, his team positions themselves as a full end-to-end commercialization partner for cell and gene therapy companies, assessing the necessary resources at the appropriate time along their commercialization journeys. 

Kevin Chinn serves as Vice President and Head of the Cell & Gene Therapy Service Line for Cencora. In his role, Kevin is responsible for leading Cencora’s strategy to support cell and gene therapy developers in commercializing their innovative products. Kevin also leads the team responsible for developing strategic partnerships with cell and gene therapy companies. Under Kevin’s leadership, his team positions themselves as a full end-to-end commercialization partner for cell and gene therapy companies, assessing the necessary resources at the appropriate time along their commercialization journeys. 

Prior to his role at Cencora, Kevin held various leadership roles at CVS Health. Most recently, Kevin was responsible for commercialization, go-to-market strategy, and sales for their Home Health division. Before his time with Home Health, Kevin led Health System Alliances, where he created mutually beneficial business relationships with provider groups and IDNs across the country, utilizing all of CVS Health’s assets. Kevin has also held sales leadership roles at Medtronic and Abbott. 

Kevin received his Bachelor of Science in Business Economics from the University of Arizona.  

Krystal Haynes

Senior Director, International 3PL Business Development, ICS

Krystal Haynes serves as the Senior Director of International 3PL Business Development for ICS. In her role, Krystal is responsible for the strategic and operational oversight of the ICS business development team, supporting manufacturers for their commercial launch, including innovative cell and gene therapies. 

With over 14 years of experience in pharmaceutical business development, healthcare, and nursing, Krystal is a seasoned corporate leader with a strong nursing background. She has excelled in various roles across Fortune 50 companies, demonstrating exceptional performance in areas such as analytics, strategic thinking, team building, and stakeholder management. Her expertise spans cell and gene therapies, commercialization, distribution, and project management, with a proven track record in enhancing customer satisfaction through effective demand and pipeline planning. She is dedicated to focusing on people and results, making her a vital asset in advancing ICS's international business development initiatives. 

Krystal holds a Bachelor of Science degree in Biology/Chemistry from Ohio Dominican University and a Master's degree in Organizational Leadership from Grand Canyon University.  



Louis Cicchini, PhD

Director, Scientific Affairs, Cencora 

Louis Cicchini serves as the Director of Scientific Affairs for Cell & Gene Therapy (CGT) at Cencora. In his strategic and educational role, he supports the development of comprehensive commercial strategies tailored to the unique aspects of advanced therapies. Focusing on improving access to CGTs, Louis collaborates cross-functionally to create innovative commercial solutions by emphasizing the clinical significance and underlying biology of these therapies, and their subsequent impact on the patient experience and product journey. Additionally, he drives external-facing CGT thought leadership initiatives, and ensures enterprise-wide alignment on CGT trends, value, and priorities by conducting field research and leading educational engagement. He is committed to fostering collaboration throughout the organization to highlight the true value of these impactful therapies with curative intent.

Louis earned his Bachelor of Science in Molecular and Cellular Biology from the University of Arizona and his Doctor of Philosophy in Molecular Biology from the University of Colorado Anschutz Medical Campus. Over the past eight years, he has dedicated his career to the fields of immunology and CGT drug development, encompassing a wide range of focus areas from research and development to clinical study planning and execution, as well as commercialization strategy and implementation. 

Malou Gemeniano

VP, Regulatory CMC, Iovance Biotherapeutics

Malou Gemeniano is VP of Regulatory CMC at Iovance Biotherapeutics, which recently announced the US approval of AMTAGVI, first tumor-derived autologous T-cell immunotherapy. Malou has over 20 years of experience in Regulatory CMC which includes experience within Industry and FDA. Her experience spans small molecules to complex biologics, such as cell and gene therapies. She was an Executive Director at Astellas Gene Therapies, where she built the Regulatory CMC team and had oversight of the regulatory CMC strategies of the AAV pipeline. At Boehringer Ingelheim, she was the US Regulatory CMC lead for Humira Biosimilar, Cyltezo. Malou has both early development and commercial experience. She began her regulatory careers while at the FDA where she reviewed earlier CAR-T programs.  

Mark Kelley

Senior Director, CGT Enterprise 

Mark Kelley serves as Senior Director, CGT Enterprise Partnerships at Cencora. In his role, Mark is responsible for new business development with Cell & Gene therapy companies. Mark’s role is to position Cencora as a full end-to-end commercialization partner for Cell & Gene therapy companies, assessing the necessary resources at the appropriate time along their commercialization journeys.

Prior to his role at Cencora, Mark held various roles at CVS Health. Most recently, Mark was responsible for business development and sales for their Home Health division. Before his time with Home Health, Mark led the Specialty Pharmacy relationships, with the world’s Blue Chip pharmaceutical manufacturers for CVS Health where he created mutually beneficial contracting relationships focused on market access and value. Mark has also held marketing and sales leadership roles at ThermoFisher Scientific, McKesson, and initially began his career with AmerisourceBergen.

Mark received his Bachelor of Arts in Communication from the University of California, San Diego and his Master of Business Administration from the University of Southern California. 

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Melissa Lattanzi

Vice President, Emerging Therapies, Cencora

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Melissa Lattanzi is Vice President, Emerging Therapies for Cencora’s Strategic Global Sourcing team. She is responsible for product access, distribution strategy, and contracting and trade relations for the cell and gene therapy and biosimilar categories.

Melissa leads business development efforts and partners with companies during clinical development on distribution and channel considerations in order to ensure commercial success. She collaborates with internal teams to ensure proper processes and infrastructure are in place to meet the unique needs of this growing category, and is a key member of the cell & gene team developing Cencora’s enterprise strategy.

Melissa joined Cencora in 2005 and has held a variety of positions spanning retail programs, full line wholesale and specialty distribution relations, channel strategy & commercialization services.


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Monica King

Sr. Manager, Regulatory Affairs, Cook MyoSite

Monica King is the Sr. Manager, Regulatory Affairs at  Cook MyoSite who has  worked in  the  public  and  private sectors. A regulatory  compliance professional who  has helped navigate FDA drug, device and biologic submissions, Monica began her career in  her hometown, at the FDA Philadelphia District office.  She worked as a  field investigator,  performing  and coordinating inspections of pharmaceutical companies,  earning a Commissioner’s  Recognition Award. Serving as a liaison for FDA and other global regulatory agencies, she led a company to  be first in the industry to file electronic Medwatch reports to CDRH. She has  also filed over 100 NDA/BLA submissions, approved without major deficiencies. At Cook MyoSite, her  focus is support for IND, RMAT submissions and associated FDA Meetings.  She holds an MBA in Marketing.  Monica currently resides in Atlanta and her hobbies include running, cooking, traveling, and  hiking with her dog Sonoma. 
Morgan Farr

Morgan Ashley Marr, MBA

National Director, Trade, Ferring Pharmaceuticals, Inc.

Morgan Farr
With over 15 years of experience in the pharmaceutical industry, Morgan brings various Therapeutic Area expertise to the table/panel.  She has spent the majority of her career in the Reproductive Medicine and Maternal Health space but over the past three years has led the entry of Ferring Pharmaceuticals into two specialized product ecosystems, microbiome and gene therapy, from a distribution perspective. 

Ferring's gene therapy entrance in the uro-oncology space is the most recent launch, however, both launches required unique distribution strategies as well as establishing distribution networks for ultra-cold chain products, whilst striving to provide a seamless customer experience.
Morgan Farr

Nancy L. Hoak​

Vice President, Account Management, Cell and Gene Therapy

Nancy is a team member of Cencora’s Cell and Gene Therapy service line and responsible for oversight of strategy development, implementation and strategic account management on behalf of the Cencora enterprise. With over 25 years of experience, Nancy joined Cencora in 2011 as Director, New Business Development supporting sales and strategy working with manufacturers to provide services to support their new product launches prior to her current role. Serving as the account lead for emerging cell and gene therapies, Nancy establishes customer relationships and oversees and coordinates a fully integrated service solution across the service lines aligned to drive the success of the launch of unique and complex cell and gene therapies for patients facing rare and complex diseases and conditions.

Prior to joining Cencora, Nancy served as a senior leader for TheraCom, A CVS Caremark Company and held a variety of clinical and leadership roles in patient and client services. Nancy as a registered nurse early in here career has held various clinical leadership positions in acute care and in home health and home infusion.

Nancy attended Millersville State University in Pennsylvania and is a graduate of Reading Hospital School on Nursing in Reading Pennsylvania.

Nathalie Boeglin 

Head of Regulatory Science for Early Stage Programs, Orchard Therapeutics 

Nathalie Boeglin holds a doctorate of Pharmacy from Paris University and 25 years of global regulatory experience with responsibilities as Global, EU and/or US Regulatory Lead gained from various positions in mid-size pharmaceutical companies (Servier, Pierre Fabre, Alexion) or as regulatory consultant (Quintiles, Voisin Consulting). Nathalie has significant scientific, technical and global regulatory expertise in the design and execution of regulatory strategies for the development up to marketing application and approval of small molecules, biologics and cell gene therapies, in various therapeutic areas and rare diseases. 

Nathalie is currently leading the Regulatory Science team at Orchard Therapeutics which is responsible for the design of global regulatory strategies and the execution of regulatory activities associated with the development of investigational ex vivo cell gene therapies in the US, UK and EU. This includes orphan and other regulatory designations or programs for expedited pathways, scientific advice and meetings with FDA, MHRA, EMA and EU national agencies, Pediatric Investigation Plans and global clinical trials for programs at various stages of development from preclinical up to the initiation of Phase 3/registrational study. 

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Rita Johnson-Greene, MBA

Chief Operating Officer, Alliance for Regenerative Medicine (ARM)

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Rita Johnson-Greene is an accomplished international healthcare executive leader with over 20 years of progressive experience. Rita is currently the Chief Operating Officer at the Alliance for Regenerative Medicine (ARM), which is the leading international advocacy organization representing the engineered cell therapy and genetic medicines sector.

Rita oversees multiple functions, including membership, finance, programming, and people and culture. She is also responsible for ARM’s geographic expansion initiative. Rita has launched three of the eight rare disease gene therapies currently marketed in the US, including Luxturna, the first FDA-approved gene therapy.


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Stephanie Wirkes

Senior Executive, Market Access, Bayer Pharmaceuticals

Stephanie Wirkes is a Senior Executive in Market Access at Bayer Pharmaceuticals US, where she leads the Distribution Team responsible for Strategy and Account Management across Trade, Specialty Distributors, Retail and Specialty Pharmacies, and Hospital GPO accounts. Her team oversees trade and distribution across a diverse range of therapeutic areas, including women’s health, hemophilia, oncology, and cell and gene therapy. Stephanie is deeply committed to ensuring that patients receive the right care at the right time and in the right place. 

Tim Hunt

Chief Executive Officer, Alliance for Regenerative Medicine (ARM)

Tim joined ARM as CEO in 2022 with more than 20 years of experience in the  biotechnology industry. A company-builder with a focus on corporate culture, he has helped early-stage organizations create internal cohesion and advance strategic initiatives. As chief executive, Tim divides his time between managing ARM and its global staff of nearly 30 employees and serving as an external advocate on behalf of ARM’s membership and the broader cell and gene therapy sector.

Tim was most recently the Chief Culture and Corporate Affairs Officer at Xilio Therapeutics, a biotechnology company developing tumor-selective immuno-oncology therapies for patients with cancer. Prior to that, he was the Chief Corporate Affairs Officer at CRISPR gene-editing pioneer Editas Medicine, where he led the company’s global policy and government affairs, bioethics, communications, market development and human resources initiatives. He also served in executive public affairs roles at Cubist Pharmaceuticals and Biogen.

Tim was an Advisory Group member of the Value-Based Payments for Medical Products consortium at the Duke-Margolis Center for Health Policy. He also has been a member of the Board of Directors of the non-profit organization Life Science Cares and has chaired the Ethics Committee of the American Society of Gene and Cell Therapy (ASGCT).

Tim is also no stranger to the ARM network. He previously served as a member of ARM’s Gene Editing Task Force and on the Biotechnology Innovation Organization’s Gene Editing Working Group.

Tim received a B.A. in history and philosophy from Boston College and a J.D. from the Columbus School of Law at the Catholic University of America. He lives in Boston with his wife and children and is a passionate fan of the Boston Celtics.

Whitley Quan, MPH 

Public Policy Manager, Cencora

Whitley Quan, a Maryland native, currently serves as the Public Policy Manager at Cencora, where she plays a crucial role in shaping health policy initiatives and legislative strategies. In her role, Whitley provides policy insights on issues related to biopharmaceutical services, strategic global sourcing, and the Medicare Drug Price Negotiation Program under the Inflation Reduction Act, influencing business decisions and identifying new opportunities. She earned her Bachelor of Science in Biochemistry from Wichita State University and holds a Master of Public Health with a concentration in Health Policy and Management from the Tulane University Celia Scott Weatherhead School of Public Health and Tropical Medicine. 

Prior to joining Cencora, Whitley was a Senior State Health Policy Analyst at Cepheid, a subsidiary of Danaher Corporation. In this role, she developed and implemented policy strategies to enhance access and equity in polymerase chain reaction (PCR) diagnostic testing across all 50 states. Her work included collaboration with companion medications to improve public health outcomes and facilitate disease prevention. 

Whitley began her career in government affairs as a policy analyst at the Louisiana Department of Health, where she significantly contributed to the successful implementation of Louisiana's Medicaid expansion under the Affordable Care Act, increasing access for millions of newly eligible beneficiaries. Earlier in her career, she gained valuable experience as an administrative fellow at The Johns Hopkins Hospital in Baltimore, Maryland. 

Whitley is proficient in policy formulation, legislative and regulatory analysis, lobbying, and patient advocacy. In her free time, she enjoys playing tennis, reading, and exploring new travel destinations. 

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