Cambridge Healthtech Institute’s 16th Annual
Strategic Resource Management
Enhanced R&D Productivity, Forecasting and Planning
October 22-23, 2018
Although investment in pharma R&D continues to increase, approval of new drugs remains relatively low. This productivity crisis presents new challenges to biopharma R&D in terms of resource management, forecasting, and capacity planning. To counteract
the decline in new therapeutics and high risk of product failure, biopharma must adapt with improved performance planning, intelligent outsourcing, and new big data analytics aimed at developing strategic and flexible resource management systems.
Cambridge Healthtech Institute’s and the BioPharma Strategy Series’ 16th Annual Strategic Resource Management: Enhanced R&D Productivity, Forecasting and Planning attracts over 100 senior R&D executives
sharing best practices and new ideas on how to enhance R&D productivity, forecasting and planning with important discussions on optimizing resource management, outsourcing, innovation, R&D, clinical capacity planning, forecasting and business
intelligence strategies.
Final Agenda
Monday, October 22
8:00 am Registration and Morning Coffee
8:50 Organizer’s Welcome
Micah Lieberman, Executive Director, Conferences, BioPharmaceutical Strategy Series, Cambridge Healthtech Institute (CHI)
8:55Chairperson’s Opening Remarks
Robert Boland, Associate Director, Emerging Science and Innovation Strategy, Johnson & Johnson
9:05 OPENING KEYNOTE & SPECIAL CO-PRESENTATION: Silo-Busting Leadership
Lauren Hirshon, Director of Operations
and Development, Leadership for a Networked World at Harvard University; Consultant, The Wharton School
Derek Newberry, Affiliated Faculty
in Organizational Dynamics, University of Pennsylvania; Author of “Committed Teams”
In an increasingly complex and volatile market environment, effective leaders must be able to fluidly work across organizational boundaries, communicate effectively with non-traditional partners, and inspire others to align around a common vision. This
is easier said than done, particularly under heightened pressure to deliver results – yesterday. In this session, we will draw on insights from anthropology, psychology, behavioral economics, and design thinking to provide a tool kit for the
new “silo-busting” leader.
10:00 CO-PRESENTATION: Ideation – Flexible Process to Support a Dynamic Book of Work
Alexander Rucci, Senior Business Capability Analyst, R&D Strategy & Planning,
Bristol-Myers Squibb
Michael Ferrante, Head, R&D Business Capabilities, R&D Strategy and
Planning, Bristol-Myers Squibb
The Ideation Module is a tool to crowdsource study ideas for the upcoming year. Indication leads representing 48 countries propose studies that are then triaged by executive leaders. This module is leveraged by our Health Economics and Outcomes Research
(WWHEOR) group. Their focus is on studies that generate data not related to a regulatory filing. The highly adaptable module provides a path to generating expenditures and planning a budget around proposed studies. The implementation of this technical
tool and business process has reduced manual work by 50% compared to prior years.
10:45 Networking Coffee Break
11:15 Creating a Performance Culture in an R&D Organization
Delfi Krishna, PhD, Director of Operations, Planning and Strategy, Cell
and Gene Therapy Platform, GSK
Does emphasizing focus on performance curb innovation in an R&D organization? With ambitious R&D agendas to be delivered under flat budgets, striking the right balance between fostering new ideas and creating a performance mindset can be very
challenging. In this case study, we will share some approaches for resourcing our organization to deliver the right priorities, for creating rigor and discipline around management of innovation and for embedding meaningful metrics to monitor performance.
We will share organizational feedback and lessons learnt.
11:45 Project Management Leadership in Drug Hunting and Drug Development
Michael Myers, PhD, Senior Director, LRL Due Diligence, Eli Lilly & Co.
This presentation will discuss: What are the transferable skills that often help to identify suspects early? What are the key differences between great organizers and great team leaders? How do you objectively squeeze the organization to do the right
thing for the program and company? How good a student are you of your company and the world’s portfolio of competition for resources?
12:15 pm Luncheon Presentation (Sponsorship Opportunity Available) or Enjoy Lunch on Your Own
(Please contact Katelin Fitzgerald +1.781.972.5458, kfitzgerald@healthtech.com)
1:40 Chairperson’s Remarks
Melquiades de Jesus, MBA, Director, R&D Strategy & Planning, Bristol-Myers Squibb
1:45 CO-PRESENTATION: Becoming an Insights-Driven Organization: How Do You Get There?
Josh Schraeder, Head of Pipeline Strategy & Management Systems
and Processes, AstraZeneca
Raveen Sharma, Life Sciences Practice Specialist Leader, Deloitte
Consulting LLP
The pharma industry struggles with being able to generate insights from its data in its strategic resource management and portfolio management functions even though large investments have been made in PPM systems and the like. In this presentation,
we will describe the journey AstraZeneca took in its GMD portfolio management function to combat data overload, data inconsistency, low adoption, and manual workarounds to arrive at a state where generating actionable insights from data easily
is the new normal. This is being achieved by leveraging an R&D Data Hub/Data Lake and data visualization and analytics configured specifically for this function.
2:15 (NEW TIME) Understanding and Addressing the Short- and Long-Term Impact of Business Development (Partnerships, Licensing, Co-Development, etc.) Agreements on Functional Resources
Josh Kaminetz, Capacity and Analytics Lead, Global Regulatory Affairs,
Merck & Co.
Business development opportunities often come with a business case that is presented as overwhelmingly positive for the company. Once the deal is signed, the celebrations and congratulations occur, then BD is off to the next deal. What remains
is an obligation to use functional area resources in support of work that was neither forecasted by the area, nor properly reflected in the business case. A case study in how this issue was addressed by our functional sub-division will be
presented.
2:45 Resource Management Made Easy
Matt Kiernan, MBA, Partner, Intrinsic Clinical Systems
With resource management, you probably fall into one of two categories – either overpaying for an over-engineered product or not even exploring options because you think they are all expensive. Intrinsic’s Insights Resource Management
will get you the resourcing information you need without driving you crazy or emptying your wallet.
3:15 Breakout Discussion Groups Remarks & Introduction to Tables and Moderators
Daniel Patrick, MBA, Director, Business Consulting, Grant Thorton
3:20 Refreshment Break with Exhibit Viewing
4:00 Interactive Breakout Discussions
Concurrent breakout discussion groups are interactive, guided discussions hosted by a facilitator or set of co-facilitators to discuss some of the key issues presented earlier in the day’s sessions. Delegates will join a table of interest
and become an active part of the discussion at hand. To get the most out of this interactive session and format please come prepared to share examples from your work, vet some ideas with your peers, be a part of group interrogation and problem
solving, and, most importantly, participate in active idea sharing. >> SEE DETAILS
- Right-Sizing Your Resource Dataset for Real-Time Capacity Planning
- Building Partnerships between Project Management, Resource Management, Functional Management, and Finance to Drive Productivity
- Resource Management: Centralized vs. Decentralized
- Developing and Leveraging Integrated Analytics for R&D
- Achieving More Effective and Real-Time Portfolio Management and Resource Allocation
- How to Leverage the PMO to Best Enable Project/Portfolio Delivery
4:40 Breakout Discussions Summary Report Outs
At the end of the interactive breakout discussions, a representative from each table will offer a summary report out.
5:00 Welcome Reception with Exhibit Viewing
6:00 Close of Day
Tuesday, October 23
8:30 am Morning Coffee
8:55 Chairperson’s Remarks
Eric Moss, MBA, Director, Portfolio & Decision Analysis, Pfizer
9:00 CO-PRESENTATION: “Target Identification” to “New Chemical Entity” in an Enterprise Planning Platform
Andrew Cheng, PhD, Business Capability
Analyst, R&D Strategy & Planning, Bristol-Myers Squibb
Michael Ferrante, Head, R&D Business Capabilities, R&D Strategy
and Planning, Bristol-Myers Squibb
We needed an enterprise solution that facilitated the planning and tracking of the drug discovery work from “Target Identification” to “New Chemical Entity.” The solution needs to support cycle-time
analysis, benchmarking, and discovery portfolio reporting. This presentation will cover how the Planisware solution provided the structure necessary to meet business needs. We will highlight design elements and strategies that allowed us to
go from design to roll-out in 5 months. This laid the foundation for integration with drug development schedules, which provides a portfolio level perspective of asset lifecycles from target identification to filing.
9:45 CASE STUDY: Optimizing Regulatory Submission Delivery Using Resource Management Tools for Capacity and Operational Planning
Pierre Roussel, DIrector, Head of GRA Demand, Capacity and
Performance Management, Vaccines Global Regulatory Affairs, GlaxoSmithKline
GSK Vaccines Global Regulatory Affairs executes over 1000 submissions each year with a team of more than 400 experts. Obtaining and providing end-to-end demand visibility is more than ever a critical success factor for on time delivery and optimal
use of critical resources. In this case study, we will share an innovative approach based on a Cloud platform for resource planning. We will share the challenges, discuss our implementation approach and share our KPI improvements.
10:15 Coffee Break with Exhibit Viewing
10:45 Sorry We Have No Time to Plan
Geert Vanhove, Founding Partner, Binocs
We often find companies in a vicious circle when they consider better resource planning processes. They want to take the initiative because there is a heavily burning platform, but… they have no time for the initiative because...there is
a heavily burning platform. I made an analysis of 3 years of resource planning implementations with Binocs to discover what works and what doesn't. With some real cases, we compiled a handful of tips that will help!
11:15 CO-PRESENTATION: Back to Basics – Case Study in the Art and Science of Resource Management
Tony Dybicz, PMP, Associate Director, Global Regulatory Affairs and Clinical Safety, Merck & Co
Jim Monahan, Associate Director, Global Regulatory Affairs and Clinical Safety, Merck & Co
Many of us have been in organizations where portfolio and resource management are taken for granted in that they’ve 'always been there'. However, some functions tend to be less mature in this space. This presentation will be a case study
of a regulatory and clinical safety organization that has evolved its resource planning from educated guesses to data-driven discussions. While the tools and fundamentals may be understood, there are change management considerations and infrastructure
that need to be built in order to make this journey.
12:00 pm Session Break, Transition to Luncheon
Strategic Resource Management & Portfolio Management Forums
12:10 Welcome Portfolio Management Conference Registrants & Joint Session Luncheon Announcements
Micah Lieberman, Executive
Director, Conferences, BioPharmaceutical Strategy Series, Cambridge Healthtech Institute (CHI)
This year, the joint keynote session will begin with a networking Welcome Luncheon and Presentation. Attendees from Strategic Resource Management and Portfolio Management are invited to enjoy a delicious plated luncheon while networking and
collaborating with fellow attendees during an informative “Lunch-and-Learn” presentation.
12:15 LUNCHEON PRESENTATION: No Excuses Portfolio Management
Richard
Sonnenblick, PhD, CEO, Enrich
Many organizations avoid formal portfolio management altogether because the data and process requirements seem arduous. But these organizations avoid portfolio management at their own peril. In this talk, we’ll provide a roadmap that
allows for a more “manageable” approach to portfolio management. I’ll review a way to classify your portfolio data requirements, how much you can accomplish with just a little data, and how to build a roadmap for portfolio
process improvements.
1:25 Chairperson’s Opening Remarks for Shared Keynote Session
Ian Popoff, Senior Director, Strategic Portfolio Management, Pfizer
1:30 Portfolio Optimization: Where Science and Business Meet
Helen Merianos, PhD, Vice President, Portfolio Management,
GSK
Determining the best investments to maximize the value of the R&D pipeline is a challenging problem because we are betting on innovation which can be hard to predict. Managing uncertainty and leveraging advanced analytics can help us make
better informed decisions. Integrating scientific insights with typical investment financials is one way to incorporate multiple perspectives and increase the likelihood of achieving your strategic objectives.
2:00 Advanced Analytics in Pharma Development: Dream or Reality?
Keith Gardner, Senior Director, Decision Science, AstraZeneca
Decision science, machine learning and artificial intelligence hold immense promise in drug development and portfolio choices. We discuss what has worked at AstraZeneca, what is coming along presently, what is on the near horizon and what
could deliver startling results. Examples include recruitment modeling, trial design and endpoint analysis, value as a function of time and competitive landscape plus complex portfolio trade-offs. AstraZeneca is leading the way toward
very sophisticated approaches using data, algorithms, opinions, modeling and guile.
2:30 Leveraging the Wisdom of the Crowd to Optimize Your Portfolio
Robert Boland, Associate Director, Emerging Science and
Innovation Strategy, Johnson & Johnson
Prediction markets and crowdsourcing have been leveraged for some time by some of the biggest companies in the world. Discover how companies such as Johnson & Johnson are leveraging these innovative approaches in unique ways to capitalize
on the knowledge of their employees, while driving strategic insights and key decision making on some of their most important portfolios.
3:00 Breakout Discussion Groups Remarks & Introduction to Tables and Moderators
Daniel Patrick, MBA, Director, Business Consulting,
Grant Thorton
3:05 Refreshment Break with Exhibit Viewing
3:45 Interactive Breakout Discussions
Concurrent breakout discussion groups are interactive, guided discussions hosted by a facilitator or set of co-facilitators to discuss some of the key issues presented earlier in the day’s sessions. Delegates will join a table of
interest and become an active part of the discussion at hand. To get the most out of this interactive session and format please come prepared to share examples from your work, vet some ideas with your peers, be a part of group interrogation
and problem solving, and, most importantly, participate in active idea sharing. >> SEE DETAILS
- Creating a Governance Body and Corporate Structure to Enable Agile Decision Making
- Making Hard Decisions: Building a Portfolio That Balances Short- and Long-Term Objectives
- Balancing Internal R&D Investments and Resources with External Collaborations
- How Do Companies Do Portfolio Management within TA’s and across the Pan-Company Portfolio?
- Right Sizing: How Can Capacity Management Contribute to Right Sizing and Outsourcing?
- Aligning Portfolio & Productivity with Corporate Strategy to Drive Strategic Resource Allocation
4:30 Breakout Discussions Summary Report Outs
At the end of the interactive breakout discussions, a representative from each table will offer a summary report out.
5:00 Close of Strategic Resource Management Executive Forum
(Portfolio Management continues through Wednesday, October 24 & Strategic and Operational Challenges of Oncology/I-O Drug Development on Thursday-Friday, October 25-26)