2024年度の講演者

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Kundini Amin, Head, Portfolio Leadership, Analytics & Insights (PLAI), Biogen

Kundini is a strategy and operations leader with more than 17 years of experience applying business acumen to pharmaceutical and biotechnology product development and partnering with leadership teams and executives to develop strategies to realize corporate objectives. Her career has spanned integrated drug development planning and execution, regulatory strategy, agency engagement and submissions, project, program, and portfolio management, business and functional strategy planning and execution, and people leadership and coaching across therapeutic areas and modalities, start ups, small and large companies, and variable portfolios. She has a Bachelors in Biology, Minor in Sociology from UC Irvine and a Masters in Quality Assurance & Regulatory Affairs from Temple University. Currently, she is the Head of Portfolio Leadership Analytics and Insights at Biogen, a team that enables disciplined actions, decisions, and changes that deliver increased short and long-term value to Biogen’s development portfolio guided and informed by enterprise strategy, new technology, and distilled data, insights, and strategic options.

Mathilde Bryse, Head of R&D Strategy, Sanofi

Currently Head of R&D Strategy, Mathilde started at Sanofi as Portfolio Strategy Director. She joined Sanofi from Vertex Pharmaceuticals, London-UK, where she held the role of Senior Manager New Product Planning. Prior to that, she was a Pharmaceuticals Equity Research Analyst at Exane BNP Paribas and previously held several Finance roles at Johnson & Johnson. As a pharmacist with a Business degree, Mathilde offers a multidisciplinary experience across Therapeutic Areas

Novartis

Stephen Cho, PhD, Senior Vice President & Head, Portfolio Strategy & Analytics, Strategy & Growth, Novartis

Stephen Cho is currently Head, Portfolio Strategy & Analytics in Strategy & Growth at Novartis. Stephen and the PS&A group manage the breadth of the Novartis portfolio across Research, Development and Commercial, including in-market brands. His group is responsible for enterprise portfolio governance, portfolio analytics and decision support, executive reporting, portfolio prioritization and review, evolving its portfolio systems to visualize and report out on the Novartis portfolio, and providing a consistent framework for long-term forecasts for in-market and pipeline assets. Stephen joined Novartis in 2012 and served most recently as Global Head of Portfolio Management & Learning in NIBR from 2019 to mid-2022. Previously he held leadership roles in Vaccines & Diagnostics, Pharma Dev, and GDD in Clinical Development, Program Management, and Strategic roles. Prior to joining Novartis, he was at McKinsey & Company where he was a leader in their Pharmaceutical and Medical Products practice, and earlier in his career, Stephen was medicinal chemistry lab head/project leader at Pfizer and a medicinal chemist at Eli Lilly & Company, where he made significant contributions to discovery and development of 5 clinical candidates and 2 marketed products across neuroscience, metabolic disorders and infectious disease areas. Stephen has a PhD in organic chemistry from Stanford University, where he studied under Prof. Barry M. Trost, and a BS degree in chemistry from the University of Michigan.

Bridging Solutions, LLC

Paul B. Cook, PhD, Principal, Bridging Solutions, LLC

Starting as a PhD academic bench scientist and professor, Paul transitioned to the life science industry consultant and program management leader working on business process projects and product development from research to commercialization. His passion is in the transition space between research and development where companies need to shape their vision and strategy.

Jazz Pharmaceuticals

Jennifer Daubenspeck, PhD, Associate Director, GMPO Systems & Integration, Jazz Pharmaceuticals

Jennifer serves as the lead for Jazz Rhythm (Planisware Timecard) and is responsible for system capabilities, processes, standards, and training. With improved timecard data, we plan to develop and enhance the resource forecasting algorithms. Prior to joining Jazz, Jennifer spent 3 years at Janssen, responsible for the development and maintenance of the resource forecasting algorithms across R&D as part of a centralized support model. Before J&J, Jennifer served in various roles with increasing responsibilities at BMS as part of the R&D operations organization. Over eight years, she supported resource forecast for the clinical operations, lead the Planisware timecard application and user group and served as the lead of the supply management database and processes. Jennifer’s first job was as an Assistant Professor, Industrial Engineering at the University of San Diego teaching introductory probability and statistics, engineering economics, and systems development and design. Jennifer has a B.S. in Mathematics from Penn State University and a PhD in Industrial & Systems Engineering from Lehigh University. She lives in Whitehall, PA with her husband, Matt, daughter Emily, and son Matthew.

Johnson & Johnson

Thomas De Vis, Associate Director Capacity Management, Johnson & Johnson

Thomas De Vis, originally from Beerse, Belgium, has forged a dynamic career path marked by a fusion of academic achievements and professional milestones. Graduating with a Bio-Engineering degree from the Catholic University of Leuven in 1999, Thomas embarked on a journey through academia, earning certifications such as APICS's Certified in Production and Inventory Management (CPIM) and pursuing specialized studies at esteemed institutions like VLERICK Management School and ENSAT. Since March 2019, Thomas has been an instrumental figure at Johnson & Johnson, serving as an Associate Director in the Portfolio, Resource, and Performance Management (PRP) department. Here, he oversees the intricate resource management of expansive portfolios, showcasing his adeptness in orchestrating data-driven methodologies and implementing artificial intelligence tools to drive transformative initiatives. Prior to his current role, Thomas held the position of Associate Director in the PMO Operational Planning and Strategy (OPS) division, where he spearheaded strategic planning processes and led business intelligence initiatives, fostering substantial cost savings and operational efficiencies. Thomas's journey with Johnson & Johnson commenced in 2005, where he began as a Manager in the DPDS Clinical Supplies Unit (CSU), progressively ascending through the ranks while leaving an indelible mark through his leadership in supply chain optimization and cross-departmental collaborations. Before joining Johnson & Johnson, Thomas contributed his expertise to Inbev as a Production & Capacity Planner and gained valuable experience at Nestlé France, where he worked on system projects within the logistics department. Beyond his professional endeavors, Thomas finds fulfillment in his familial roles as a devoted husband and father of two. His leisure pursuits, including cycling and football, reflect his active lifestyle, while his commitment to community and environment is evident through his involvement in initiatives like the creation of a food forest and coaching his daughter's hockey team. Additionally, his passion for music shines through his role as a pianist, where he brings joy to individuals with mental disabilities through his performances. Thomas De Vis epitomizes a harmonious blend of professional excellence, personal enrichment, and altruistic endeavors, shaping a narrative defined by resilience, innovation, and compassion.

Michael Ferrante, Executive Director, Business Analytics, Global Regulatory Affairs & Clinical Safety, Merck

Michael Ferrante is the Executive Director, Business Analytics, Global Regulatory and Clinical Safety (GRACS) within Merck Research Labs. In this role, Mike is responsible for tracking and analyzing time reporting effort, forecasting resources for 1-5 years, prioritizing the portfolio, and aligning metrics and analytical tools for the 2500-person global organization. Mike was most recently Head, R&D Business Capabilities, at Bristol Myers Squibb in Princeton, where he led the R&D project, portfolio, clinical study management and headcount planning capabilities. Before joining BMS, he served as Managing Director of Consulting Solutions at YourEncore. Mike previously worked at Merck, where he was Senior Director, Business Operations, supporting clinical grants planning and budgeting, functional objectives development and execution, and strategic analysis for global clinical development and regulatory. He also led R&D operations for Merck’s subsidiary in Japan. Mike earned a B.S. in Chemical Engineering from the University of Michigan, an M.S. in Chemical Engineering from Carnegie Mellon University and an MBA from the Ross School of Business at the University of Michigan. He lives in Cranbury, New Jersey, with his wife Deanna and have two grown children.

Eli Lilly and Company

Stuart Fort, Senior Director, Project Management Strategy and Capabilities, Eli Lilly and Company

Stuart Fort is Senior Director in the Project Management Strategy and Capabilities group with 34 years of experience at Eli Lilly and Company. His career spans process development, technical leadership, capacity and strategic resource management, resource modeling, and project/portfolio reporting and analysis. He earned Bachelor of Science degrees in Chemistry and Chemical Engineering from Purdue University and an MBA from the University of Phoenix. He is a licensed Professional Engineer in the State of Indiana and holds a CPIM certification from APICS.

Janssen Pharmaceuticals Inc

Sean Gallagher, Director, Capacity Management and Business Analytics, Johnson & Johnson

After graduating with a BA in Biology, Sean briefly taught Biology and Physical Science at Kensington High School in the School District of Philadelphia. He then went on to join the Bioprocess and Bioanalytical Research department at Merck & Co., Inc. where he spent almost eight years working in the field of Vaccine R&D working on projects such as GARDASIL, RECOMBIVAX, VAQTA, and several pre-clinical vaccine candidates. In 2008 Sean completed both his MS and MBA at Drexel University and made the leap from Bench-to-Business joining the Resource and Decision Management team in the Merck PMO. In 2012, Sean moved to the PMO at Janssen R&D where he increased his breadth of PM knowledge across multiple disciplines and now leads a team of Capacity Managers. Sean and his wife Kim spend most of their time outside of work hiking and fishing with their two beagles Isaac and Linus.

Andrea James, Senior Director, Head of Portfolio Resource Forecasting, Merck

Andrea has over 20 years of experience within the healthcare industry across the disciplines of strategy, project, portfolio, and resource management. She has worked for organizations such as the Centers for Disease Control and Prevention, Merial Limited, Eli Lilly, Boehringer Ingelheim, and Roche. In her current role as Head of Portfolio Resource Forecasting for Merck, her responsibilities include strategy, management, and governance of resource forecasting, capacity management, and related systems and tools. Andrea holds a Master of Science in Immunology and a Bachelor of Science in Medical Microbiology from the University of Wisconsin. Andrea completed the Project Management Professional certification and has a Lean Six Sigma Black Belt certification.

Josh Kaminetz, GRA PPMO Lead, Takeda

Josh Kaminetz is the PPMO lead for Takeda’s Global Regulatory Affairs. His small team manages and supports the portfolio of change projects for GRA, which enable the organization to operate efficient, effective, and compliant business processes. Josh has a 30+ year professional career in the pharmaceutical industry. After earning a Bachelor’s of Science degree in Chemistry from the University of Richmond, he spent his early career as a bioanalytical chemist and laboratory manager for a CRO in Richmond, Virginia. Shortly after achieving a Master’s of Business Administration degree at Virginia Commonwealth University, he joined Merck Research Laboratories, where he held operations management roles partnering with a variety of senior leaders in both Discovery and Early Development and Regulatory Affairs. Josh moved to a role in Merck’s Corporate Strategy group where he was on the core team to stand up and spin off Organon. Post-spin, Josh stood up and led the R&D Portfolio, Project, and Resource Management capabilities at Organon before joining Takeda in his current role.

Elayne Ko, Director, Portfolio Decision Sciences, GSK

Elayne Ko has 20 years of experience in applying decision analysis process, tools, and methodologies to facilitate investment decision-making under risks and uncertainties. Her work focuses primarily in the pharmaceutical industry; in particular, drug development decisions, long-term planning, and disease area/portfolio prioritization. She has worked with R&D teams to develop business case recommendations, and with senior management who makes investment funding decisions. Elayne has gained experience - in consulting and in corporate settings - across several industries including healthcare information technology, oil & gas, and mining.

EMD Serpmp

Ivan Kugener, VP & Head Global Portfolio Mgmt, Valuation & Analytics, EMD Serono

Educated as a Medical Doctor, Board certified I supplemented my education with an MBA and a Master in Mathematics. I started my career in the French Navy where I reached the rank of Captain at 25 years old. I spent over 7 years at Abbott Laboratories (90-97) and nearly 5 years at Medtronic (97-01). For 7 years I worked at a private Swiss bank (Lombard Odier Darier Hentsch) where I managed (with a team of five reporting to me) more than USD2bn invested in healthcare private and public equities. I then drove the mid-long term strategic effort for EMD Serono, the US subsidiary of Merck-Serono. I then headed the Medical Affairs at Arthrocare (sold to Smith & Nephew for 1.3 billion). I now head the pharmaceutical portfolio management and decision science function at Merck, as well as R&D Governance and resource management.

Tilburg University

Christopher Larson, Tilburg University

Christopher Larson is Director of Portfolio Program Management at AbbVie. Christopher has diverse experience in program management, portfolio analytics, decision science and finance. He is currently pursuing a PhD in Finance at Tilburg University. His presentation is based on original PhD research focusing on R&D organizational choices and innovation performance in the biopharmaceutical industry.

Johnson & Johnson Innovative Medicine

Sabine Lenders, Associate Director, Capacity Management, Johnson & Johnson Innovative Medicine

As Associate Director Capacity Management at J&J, I act as a trusted advisor for senior leadership in delivering business insights related to capacity management and resource utilization to drive strategic decision-making. With a background in Strategic Partnerships spanning 3.5 years, I've honed my skills in fostering collaborative relationships and identifying synergistic opportunities. My passion lies in maximizing operational efficiency by leveraging internal strengths and strategic alliances.

Alnylam Pharmaceuticals

Leslie Lippard, Senior Director, Portfolio Analytics, Alnylam Pharmaceuticals

Leslie Lippard joins us from Alnylam, where she is Senior Director, Portfolio Analytics. Leslie has been working in the portfolio space since 1995. Prior to Alnylam, she was part of Genentech’s research and early development pipeline and portfolio planning group in San Francisco. She has a broad background in the pharma portfolio space, and has consulted at Pfizer, Amgen, Abbott/Abbvie, Genentech, JNJ, and Mallinckrodt Medical. She’s also worked in market research, collecting information used to support portfolio and other decision making, founded two successful companies to provide those services, and has worked in project management at Intermune. She’s currently the President of the Society for Decision Professionals, and a frequent contributor to the Decision Analysis Affinity Group Conference. She has been involved in the leadership of the San Francisco Chapter of the Healthcare Businesswomen’s Association and looks forward to becoming involved in the HBA in Boston. She has a BS in Physics from Caltech and an MBA from the University of Oregon (Go Ducks!). Outside of work, you are most likely to find Leslie exploring Boston on foot with binoculars and a sketchpad or in the pool swimming laps.

Intelligencia.ai

Edoardo Madussi, Head of Business Development, Business Development , Intelligencia.ai

No bio available.

Eli Lilly & Company

Michael Myers, PhD, Associate Vice President, LRL Project Management-Due Diligence, Eli Lilly and Company

Dr. Mike Myers has worked >30 years in pharma and has spent his career contributing to the discovery and development of new drugs. He is an inventor on 35 patents and has led teams in the pursuit of innovative treatments for cancer, CNS, infectious and cardiovascular disease. Mike is currently Sr. Director LRL Project Management - Due Diligence and is involved in Lilly’s activities as part of the larger External Innovation team.

AstraZeneca

Charles Naaman, Vice President, Global Portfolio & Project Management-Oncology, AstraZeneca

No bio available.

Panzano Enterprises LLC

Mary Lou Panzano, Founder and CEO, Panzano Enterprises LLC; former Vice President, Internal Communications, Bayer

Mary Lou Panzano is founder and CEO of Panzano Enterprises, where she focuses on helping leaders prosper in times of change and beyond. She is a communications executive with over 30 years of experience leading successful programs to support transformational change initiatives at global companies. She served as vice president, internal communications at Bayer, and held senior communications roles and Pfizer and Prudential. Today, she is a highly-sought-after speaker, coach, and author. Her 4Cs Change Framework and article series, “The 11 Principles of Prosperity,” are change-maker success essentials.

Eli Lilly & Co

Charles Persinger, Executive Director, R&D Strategy & Decision Sciences, Eli Lilly and Company

Charles Persinger is an Executive Director in R&D Strategy at Eli Lilly and leads their Decision Sciences group. He joined Lilly after receiving his MBA from Duke University. Charles has over 20 years of experience helping enable organization decision quality at Lilly, with a focus on drug development and portfolio management decisions within Research and Development. He and the Decision Science team at Lilly work directly with decision-makers and drug development teams to enable decision quality across the R&D organization through a combination of direct decision consulting, developing and enabling decision processes, and education efforts.

Novartis

Peter Ray, Vice President, Head of Portfolio Analytics, Novartis

Peter is a life sciences executive with a unique perspective on the R&D productivity and sustainability challenges facing biopharma companies at different stages of their evolution, and deep knowledge of the enterprise capabilities needed to address them. He has extensive experience in translating data and analytics into value-creating and optimizing strategies at the asset, franchise, and portfolio level, and he is an expert in characterizing and assessing risk and uncertainty. He has led process and organizational redesign efforts, integrating and collaborating across functions to improve both the speed and quality of decisions.

Sumitomo Pharma America, Inc.

Alexander Rucci, Director, Project Management, Sumitomo Pharma America

Alex most recently served as Associate Director, Business Capability at Jazz Pharmaceuticals. He also leads the process development and business engagement for Jazz’s project planning tools, including Planisware™, Box™ and PMO Tableau™ reports. He is responsible for managing capacity planning data outputs for all functions in R&D. Capacity Planning data supports functions by identifying bottlenecks, estimating increased effort for new projects, and headcount planning. It also supports Project Teams by bringing transparency to cross-functional effort, as a quality check on the project plan, and supports overall project cost estimation. This data is also highly leveraged by Governance to plan R&D headcount and prioritize work across departments. Prior to joining Jazz, Alex supported many functions across Bristol Myers-Squibb in their use of Planisware. From leveraging the Ideation module to support study planning in Medical Affairs to Resource Management algorithm support to foundational project planning support, BMS is where he gained his foundational Planisware experience. Prior to that he validated drug packaging rooms, equipment, materials, and processes at Xerimis. This was his first experience in pharmaceutical development and where he discovered how much he enjoys working in the drug industry. Alex earned a B.A. in Pure Mathematics from Rutgers University, Camden and an M.E. in Chemical Engineering from Rutgers University, New Brunswick. He lives in Burlington City, New Jersey with his wife, Colleen and their two sons, Leo and Max.

Innovate in What You Do! LLC

Michelle Shogren, CEO & Owner, Innovate in What You Do!; former Senior Director of Innovation, Pharma R&D Clinical Operations, Bayer

Michelle Shogren, CEO of Innovate In What You Do! LLC boasts 25+ years in clinical research, beginning as a patient participant. Her journey led her through roles in nursing, monitoring clinical trials, and a pivotal tenure at Bayer Pharmaceuticals. Michelle's innovation-driven career culminated in founding her own innovation company in 2022. She's passionate about revolutionizing clinical trials, promoting user voice, and fostering innovation in healthcare.

Zentalis Pharmaceuticals

Joe Stalder, Vice President, Program Management, Zentalis Pharmaceuticals

Joe Stalder, PharmD, PMP, is Vice President of Project Management at Zentalis in San Diego, CA, co-founder of Groundswell Pharma Consulting, and editor of the book "Project Management for Drug Developers." Joe has over 10 years of project management experience in pharmaceutical development in large and small companies. His experience includes Project Management department head, PMO head, and Lead Project Manager on several early- and late-stage development assets in oncology, infectious disease, cardiology, metabolism, and pulmonology. Joe is also a regular speaker at biopharma PPM conferences and is involved in biopharma PPM community organizations including PIPMG and BiopharmaPM.

Gary J. Summers, PhD, Director Oncology Portfolio Decision Sciences, Strategy Portfolio Management, GSK

Gary Summers is a Director of Oncology Portfolio Decision Sciences at GSK, where he applies decision analysis to drug development. Complimenting this work, Dr. Summers studies how uncertainty impacts decision-making. His paper, “Friction and Decision Rules in Portfolio Decision Analysis,” won the 2021 Clemen-Kleinmuntz Best Paper Award. Dr. Summers earned an M.S. and Ph.D. in Management Science from Northwestern University.

Mr. Dan Tierno has over 25 years of experience in portfolio management, drug development, mHealth, clinical trial design, big data and cell and gene therapy. Mr. Tierno has spoken on training scientists for rare disease therapeutic development, innovations in cell and gene therapeutic development and defining and generating value via portfolio management. Mr. Tierno holds his Honors MBA from the Zicklin School of Business at Baruch College, and his MA in Biotechnology from Columbia University.

AbbVie Inc

Gregory Wayne, PhD, Head, Decision Sciences Group, AbbVie, Inc.

Greg leads the Decision Sciences Group (DSG) at AbbVie. DSG enables clarity of action through economic analysis, insights, and facilitative leadership for its business partners dealing with complex issues and trade-offs. Greg advises AbbVie’s senior R&D leaders on portfolio and resource investments. He has over 25 years’ experience in the pharma and medtech industry, with prior roles in drug development, program management, corporate strategy, and business integrations. He received his PhD in chemistry from the University of Chicago and his MBA from the Kellogg School of Management at Northwestern University.

Caribou Biosciences Inc

Saeid (Sam) Yazdani, Principal Consultant, Yazdani Consulting; former Vice President of Portfolio & Program Management at Caribou Biosciences

Saeid (Sam) Yazdani is a result-focused executive with over 20 years of experience in global drug discovery and development. As the Vice President of Portfolio & Program Management, he has been instrumental in advancing complex drug development programs, securing multiple FDA approvals, and leading cross-functional teams from discovery through commercialization via a patient-centric mindset. Saeid is known for his strategic vision, execution excellence, and ability to drive innovation through rigorous stage-gate governance. His expertise spans preclinical and clinical operations, with a proven track record of managing significant R&D budgets and delivering high-impact results. His tenure includes companies such as Pfizer, Gilead, Genentech, Merck, Nestle Health Sciences, Thermo Fisher, and Caribou Biosciences. Saeid holds an MBA from the University of Southern California, a BS in Chemistry from Western Michigan University, and is certified in Six Sigma Black Belt and Project Management.

Jazz Pharmaceuticals

Melquiades de Jesus, Senior Director, R&D PMO Business Capabilities, Jazz Pharmaceuticals

Mel serves as the business owner for Jazz's enterprise project & resource management system, Planisware™. His team is responsible for the drug development project management process, the “functional book of work,” resource forecasting in support of the annual and portfolio processes. This is achieved by advocating the development and adoption of business processes and tool enhancements that promote and support good project management practices, accurate resource forecasting informed by timecard data. Prior to joining Jazz, Mel served as Planisware business owner at BMS, were he led his team in standardizing the project, resource management and time tracking processes across 5 therapeutic areas, reducing the budget cycle process by 30% while increasing transparency and accuracy of dates and forecasts. At Merck, he led the preclinical functional planning teams. He served as a Senior management consultant for PricewaterhouseCooper (PWC) and managed the pharmaceutical development technology transfer team to successfully introduce 3 new products at Barceloneta, Puerto Rico for Abbott Labs. Mel earned a B.S. in Pharmacy from Rutgers University and a MBA from Columbia Business School. He lives in Yardley, Pennsylvania with his wife, Stephanie, and their two daughters, Sophia and Olivia.

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Program and Portfolio Management

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