15-16 November 2023
Wed-Thurs
New York Marriott at the Brooklyn Bridge, USA

USA Clinical Trials Innovation
& Outsourcing Programme

Event Schedule

Have a look at Schedule

08:00

Registration & Itinerary Collection

08:50

Opening Remarks

Amraj Dhillon

Key Account Manager

World BI
08:55

Chairperson Welcome Address

Joe Stauffer

Chief Medical Officer

Antibe Therapeutics Inc.
09:00

Presentation 1: Application and Challenges of Bioinformatics Technologies in Clinical Trials

OhKyu Yoon, PhD, MBA

Head of Oncology, Clinical Bioinformatics & Exploratory Analytics

Gilead Sciences
09:25

Presentation 2: Monitoring Cognitive and Everyday Function with Digital Endpoints in Decentralized Clinical Trials

John Bernstein

Clinical Scientist

Cambridge Cognition
09:50

Presentation 3: The Case for a Centralized Ancillary Supply Function as part of the Clinical Supply Chain

Doug Meyer

Sr. Director, Clinical Supply Chain

Takeda
10:15

Coffee Break & Networking Session

11:05

Presentation 4: How to gather patient input to inform product development and enhance data collection and analytics

Deborah Collyar

Founder and President

Patient Advocates in Research (PAIR)
11:40

Presentation 5: Patient Recruitment Acceleraltion

Jose Puerto

Managing Partner

Credent Partners USA
12:10

Presentation 6: Trends & Challenges in Pharma Sourcing and Procurement – External Manufacturing as the "Procurement's Operational Arm"

Luiz Alberto Barberini

External Manufacturing Organization - Consumer Health LatAm ; Community Board Chair at CSCMP

Bayer
12:45

Networking Lunch

13:45

Presentation 7: Drivers of Waste in Clinical Supplies


  • Understand the average waste level in the industry
  • Explore the drivers of waste in clinical supplies
  • Learn how early planning and continuous monitoring can enhance clinical supply chain efficiency

Maxime Derep

Senior Solutions Engineer

N-Side
14:10

Give and Take Chat: Improve quality performance in clinical supply & Implementation of Lean supply chain

Moderator

Doug Meyer

Sr. Director, Clinical Supply Chain

Takeda

Luiz Alberto Barberini

External Manufacturing Organization - Consumer Health LatAm ; Community Board Chair at CSCMP

Bayer
14:40

Coffee and Networking Break Session

15:30

Presentation 8: The importance of diversity in clinical trials

Bianca Green

Diversity & Inclusion in Clinical Trials Senior Manager

Takeda
15:55

Give and Take Chat: Enhancing diversity and inclusion in clinical trials

Moderator:

Melissa Penn

Director, Patient Engagement R&D

Bayer

Panelist:-

Bianca Green

Diversity & Inclusion in Clinical Trials Senior Manager

Takeda
16:30

Chair Closing Remarks

Joe Stauffer

Chief Medical Officer

Antibe Therapeutics Inc.
16:55

End of Day 1

08:00

Registration & Itinerary Collection

08:50

Opening Remarks

Amraj Dhillon

Key Account Manager

World BI
08:55

Chairperson Welcome Address

Shrividya Iyer

Executive Director, Oncology Worldwide Real World Evidence (RWE) & US HEOR

Eisai US
09:00

Presentation 9: Technology adoption: Adoption of tools that support clinical trial execution

Maria I Florez

Research Consultant

Tufts Center for the Study of Drug Development
09:25

Presentation 10: Using integrated network of real-world data to optimize clinical trials operations

Joe O’Rourke

Head of Commercial Development

Walgreens Clinical Trials
09:50

Give and Take Chat: Ways to get RWE, which are useful for making drug approval decisions

Moderator

Shrividya Iyer

Executive Director, Oncology Worldwide Real World Evidence (RWE) & US HEOR

Eisai US

Joe O’Rourke

Head of Commercial Development

Walgreens Clinical Trials
10:20

Coffee Break & Networking Session

11:10

Presentation 11: Direct Data Connection: an EHR to EDC cloud-based platform

Amir Emadzadeh

Director of Software Engineering

Genentech
11:35

Presentation 12: Preparing for Digital Transformation: Implications for Supply Chains and Clinical Trials

Randy V Bradley

Associate Professor of Supply Chain and Information Systems Management

The University of Tennessee
12:00

Give and Take Chat: Stability aspects of clinical supplies

Moderator:-

Randy V Bradley

Associate Professor of Supply Chain and Information Systems Management

The University of Tennessee

Panelist:-

Chidi Umeh, MBA, ASQ-CQA

Director of Quality

Telios Pharma, Inc.
12:30

Networking Lunch

13:30

Presentation 13: Analytical support for Clinical Trials

Anka G. Ehrhardt

Director, Cell-Based Assays / Analytical Research & Development

Merck
13:55

Presentation 14: Addressing Disparities in Clinical Trials: Ensuring Inclusivity and Equity in Medical Research

Benji Etienne

Senior Manager, Clinical Research Sourcing Strategist

Pfizer
14:20

Chair Closing Remarks

Shrividya Iyer

Executive Director, Oncology Worldwide Real World Evidence (RWE) & US HEOR

Eisai US
14:30

End of Conference