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Thinking Bigger, Acting Bolder

ANNUAL REPORT 2024

A Message From CEO Janice Chang

2024: A pivotal year for TransCelerate

We turned bold visions into action as we worked toward our goal of converging clinical research with patient care.

This mission is deeply personal to me.

Years ago, I lost my father. I often wonder if a clinical trial could have changed the outcome.

This drives my passion for our work, and I’m delighted by our progress over the past year.

We are committed to improving the experience for every patient waiting for a breakthrough.

Together, we’re building a better future for clinical research.

One that is more connected, efficient and
patient-centered.

“Every patient waiting for a breakthrough fuels our mission to transform clinical research.”

Thinking Bigger

Our Vision for the Future

We’re thinking bigger, addressing systemic challenges and accelerating innovation.

At TransCelerate, we strive to:

Seamlessly connect clinical research and patient care

Make vital trial information easily accessible

Deliver life-saving medicines faster and safer

Our approach combines rapid improvements for immediate implementation with long-term solutions to transform the R&D ecosystem.

How we make it happen:

Collaboration

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20+ leading biopharma companies join forces

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Cross-Functional
Expertise

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Diverse
skills power initiatives

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Neutral
Platform

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Non-profit
structure encourages open collaboration

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Strategic
Partnerships

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Key
collaborations across R&D ecosystem

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These pillars support our three key focus areas:

Transforming Connectivity 
Redefining how research
and care interact

Information
Sharing & Reuse

Leveraging existing data
for faster discoveries

Innovative
Trial Design

Putting patients at the heart of clinical trials

Catalyzing Progress in Clinical Research

Since 2012, we’ve grown from a startup team with five initiatives to a transformative force in biopharma R&D.

20+

member companies

35+

tools and solutions
in progress

570+

toolkits delivered

700+

benefits realized

But the true value can’t be measured by numbers alone. We’re effecting positive changes by driving:

Efficiency

Faster, more streamlined processes

Quality
Higher standards to enhance clinical trial integrity

Speed

Quicker delivery of 
treatments to patients

Experience
Enhanced experiences for both patients and researchers

Driving Change from the Top

Our board of directors balances visionary ambition with practical execution, guiding us to take on bold challenges while delivering tangible outcomes.

“The mission of TransCelerate and the role we can collectively play in advancing positive change has never been more important. With the strategic direction that we have set and our track record of delivering tangible, meaningful solutions, I am extremely confident about what we can accomplish next.”

Robert Metcalf 

Group Vice President, CDDA, 

China & Japan Medical, Eli Lilly & Co.

Transformation from Within

Our member companies are at the core of TransCelerate’s success.

They invest $125+ billion

each year to bring new medicines to market.

They report more than 700 benefits across key categories, including:

SPEED
EFFICIENCY
QUALITY

“TransCelerate has really become part of our language at Amgen. Any of my colleagues here today would emphatically agree: the collaboration with TransCelerate has changed how we work as a company."

Narimon Honarpour,
M.D., Ph.D., 


Senior Vice President,
Global Development at Amgen

Tackling Key R&D Ecosystem Challenges

R&D at the speed of innovation? That’s our goal.
Together, we’re solving critical challenges to accelerate answers for patients. Some highlights:

SOLUTION
Digital Data Flow aims to modernize trials by digitizing protocols, automating data flow and streamlining the R&D process, reducing cycle times and improving data quality.

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CHALLENGE

Inefficient data flow slows the delivery
of new and potentially life-saving treatments to patients.

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SOLUTION
Historical Trial Data Sharing enables companies to improve study design, reduce placebo use and accelerate drug development by responsibly and securely sharing and reusing data.

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CHALLENGE

Missed opportunities to advance scientific decision-making due to the siloed nature of existing data.

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SOLUTION
The Modernizing ICSR Management initiative seeks to transform the Individual Case Safety Report system, reducing duplication, enabling real-time safety data access and enhancing patient safety through more efficient processing.

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CHALLENGE

Global regulatory complexity can hinder efficient safety monitoring and timely treatment delivery.

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SOLUTION
The Embedded Pragmatic Trials initiative will facilitate the ability to conduct pragmatic clinical trials by developing resources, proving feasibility and addressing operational differences to better integrate research into routine care.

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CHALLENGE

Traditional clinical trials and regulatory complexity regarding real-world evidence limit the application of research to patient-focused care.

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SOLUTION
The Modernizing Clinical Trial Conduct initiative advances trials by helping companies adopt patient-friendly technologies like telemedicine, offering more flexibility while ensuring patient safety and data integrity.

SOLUTION
The Modernizing Clinical Trial Conduct initiative advances trials by helping companies adopt patient-friendly technologies like telemedicine, offering more flexibility while ensuring patient safety and data integrity.

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CHALLENGE

Complicated protocols and burdensome visits can make clinical trials less patient-friendly, limiting diversity and real-world insights.

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The work is important, filled with victories and setbacks, but our resilience and belief keeps us moving forward.

Collaboration in Action

In 2024, we forged partnerships that are redefining collaboration across R&D.

EU-Pearl Logo

EU Patient-Centric Clinical Trial Platforms
Partnering with European health consortium to simplify approach to patient-friendly platform trials

Association of Clinical Research Organizations (ACRO)
Co-creating tools to support the implementation of new Good Clinical Practice guidelines around the world

CDISC-logo

Clinical Data Interchange Standards Consortium (CDISC)
Accelerating development of clinical data exchange standards for protocol digitization

We engaged in productive dialogue and action with global health authorities to accelerate the pace of change.

Implemented a holistic approach to engage with health authorities worldwide

Actively participated with health authorities at conferences and public events

Advanced knowledge and educated health authorities through sharing of insights, learnings and data

Our insights made waves across the R&D ecosystem.

10 public webinars reached
4,000+ professionals

White papers tackled everything from decentralized trials to real-world data

Featured in top publications from DIA Global Forum to Applied Clinical Trials

TransCelerate’s Expanding Presence

In 2024, we shared our voices at over 40 leadership-level events across 27 cities and 12 countries.

Hosted member meetings with industry leaders across three continents
Featured in key sessions at DIA, SCOPE and Milken, among others
Engaged with global health authorities and international trade associations
Hosted member meetings with industry leaders across three continents
Featured in key sessions at DIA, SCOPE and Milken Future of Health Summit
Engaged with global health authorities and international trade associations

Looking Ahead

As TransCelerate looks ahead, we’re exploring the transformative movements that have the potential to reshape biopharma R&D. This includes technological advancements enabling better data interoperability, improved data quality and risk detection and the expansion of access to treatment through the convergence of clinical research and care.

Together, we’re building a more efficient, patient-centered future for clinical research.

For a deeper dive into our work, download our full report here.

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