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Live Oral Poster Presentations III
Learning Objective : •Provide an understanding of the climate impact of clinical research •Discuss opportunities to develop a more robust understanding of key sources of greenhouse emissions in our trials, and create opportunities for benchmarking and sharing of best practices •Provide insights into how we can position sustainability to co-inform clinical trial design based on real world experiences of trial sponsor
Speaker(s)
Ensuring the Benefits of Our Therapies are not Offset by Our Operations: Reducing the Climate Impact of Clinical Research
Jason LaRoche, MSc
Director, Innovative Health, Johnson & Johnson Innovative Medicines, Netherlands
Megan Heath, PhD
Head of Clinical Study Units Europe Region, Sanofi, United Kingdom
Towards Equitable Participation in Oncology Trials: Evaluating Eligibility-Based Representativeness for Black Patients
Corey Michael Benedum, PhD, MPH
Quantitative Scientist, Flatiron Health, United States
Lidewij Eva Vat, DRSc, MS
Program Director, The Synergist, Netherlands
Bringing eConsent to the Place it Deserves through Harmonizing and Insights in Value Models
Hilde Vanaken, PhD, MSc
Head, European Forum GCP (EFGCP) eConsent Initiative, Head TCS Industry Leaders, EFGCP, TCS, Belgium
Systematic review of externally controlled (EC) trials, data used in them, and their role in regulatory decision-making
Sini Eskola, MPharm, MSc
PhD Candidate, University of Utrecht, Netherlands
Qualitative analysis of participant-entered free text data to inform good diary design
Saima Khakwani, MPH, MSc
Clinical Science Associate, Clario, United Kingdom
Lisa Ensign, PhD, MSc
VP, Statistics and Regulatory Science Innovation, Medidata, a Dassault Systemes Company, United States
Evaluating an algorithm for fit-for-purpose use in feature extraction of motor function in early-stage Parkinson’s disease.
J. Rubin Abrams, PhD
Quantitative Medicine Scientist, Critical Path Institute, United States
Isabelle Huys, PharmD, PhD, MPharm
Professor, KU Leuven, Belgium
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