SCOPE News & Media

Medical Device Reimbursement Strategy: How to Plan for Successful Market Commercialization
Author: Edward Black, Director of Global Reimbursement Strategy, NAMSA
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Defining a Central Monitoring Capability: Sharing the Experience of TransCelerate Biopharma's Approach, Part I.
Co-Authors:
David Knepper, Head, Continuous Improvement, Forest Laboratories
Andy Lawton, Global Head, Data Management, Biometrics & Data Management, Boehringer Ingelheim Ltd.
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Technology Considerations to Enable the Risk-Based Monitoring Methodology
Contributing Author: Shelly Barnes, Senior Project Manager, Global Clinical Solution Center – Strategy and Innovation, Sanofi
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Interviews

January 25, 2021 Clinical Research News
Risk Management During A Pandemic: How Pfizer’s Quality Management System Fared, an interview with Melissa Suprin, Head, Quality Risk Management, Clinical Development, Pfizer, Inc.

January 10, 2020 Clinical Research News
Transformational Change To The Supply Chain an interview with Matthew Moyer, MS, MBA, PMP, Director, Clinical Supply Technology, Global Clinical Supply, Merck & Co., Inc.

December 10, 2019 Clinical Research News
Real World Evidence And European Regulations an interview with Jennifer Bolton, Senior Fellow, Regulatory Affairs, Boston Scientific Corporation

February 13, 2019 Clinical Research News
Clinical Trials In The Age Of Data Marina Filshtinsky, Executive Director of Conferences at Cambridge Healthtech Institute

February 2019 Yprime Blog Post
SCOPE 2019 Summary – Beyond the Pilot, Moving Towards Implementation Donna Mongiello, RN, BSN, Vice President Strategic Solutions, YPrime

February 12, 2019 Clinical Research News
IRT Developers, Engineers See The Patient Beneath The Data an interview with Andrew Rohrbaugh, Director of Client Delivery at Cenduit

February 7, 2019 Clinical Research News
Doing More With Less: The Road To Success For Clinical Trials an interview with Rosie Filling, Vice President of Clinical Development Operations at Endo

February 5, 2019 Clinical Research News
The Informed Patient: How Biosample Management Is Evolving For Consent an interview with Caoimhe Vallely-Gilroy, head, Clinical trial biosample management and informed consent at Merck KGaA

February 1, 2019 Clinical Research News
How Real World Data Changes Clinical Trials, And What That Means For Patients an interview with Martin Marciniak, US Medical Affairs Vice President, leading the Customer Engagement Value Evidence and Outcomes Team at GlaxoSmithKline

January 31, 2019 Clinical Research News
Real Risk, Real Quality: Risk-Based Monitoring In Clinical Trials Today

January 28, 2019 Clinical Research News
A Realist Looks At AI In Clinical Trials an interview with Ronald Dorenbos, Associate Director Materials & Innovation, digital strategies group for neuroscience at Takeda

January 11, 2019 Clinical Informatics News
The Future Of Real World Data In Clinical Trials an interview with Cathy Critchlow, Vice president and head of the Center for Observational Research, Amgen

January 9, 2019 Clinical Informatics News
Starting Line: How To Begin Getting Patient Input Into Clinical Trial Design an interview with Beth Zaharoff, Director of patient-focused clinical trial engagement at TESARO

How Real World Data Changes Clinical Trials, And What That Means For Patients
With: Martin Marciniak, PhD, Vice President, US Medical Affairs, Customer Engagement, Value, Evidence & Outcomes, GSK
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Real Risk, Real Quality: Risk-Based Monitoring In Clinical Trials Today
With: Andy Lawton, Director & Consultant, Risk Based Approach Ltd.
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A Realist Looks at AI In Clinical Trials
With: Ronald Dorenbos, PhD, Associate Director, Materials and Innovation, Takeda Pharmaceuticals
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Are We Ready for AI In Clinical Trials?
With: Francis Kendall, Director, Biostatistics & Programming, Cytel, Inc.
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Preparing CRAs to be Site Recruitment Managers: The Pros, the Cons and The Process
With: Beth Harper, President, Consultant, CPP, Inc.
Nikki Christison, President, Consultant, Clinical Resolutions, Inc.
Gretchen Goller, Senior Director, Patient Access and Retention Services, PRA International
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Kelly Zou: Mathematics, Statistics, Data Science, and Dreams
Kelly Zou, Ph.D., PStat®, Senior Director and Analytic Science Lead, Real World Data & Analytics (RWDnA), Global Health & Value (GH&V), Pfizer, Inc.
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Kelly Zou: Meet Inspirational Women in Statistics & Data Science
Kelly Zou, Ph.D., PStat®, Senior Director and Analytic Science Lead, Real World Data & Analytics (RWDnA), Global Health & Value (GH&V), Pfizer, Inc.
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Podcasts

View a Transcript of the Podcast here

Clinical Trial Contracting Challenges: Streamlining CTA Negotiations Beyond Legal Language

Débora Araujo, Associate Director, Site Budgets and Payments (US Group Head), Boehringer Ingelheim Pharmaceuticals, Inc.

Débora Araujo of Boehringer Ingelheim spoke to CHI to discuss her expertise in clinical trial agreements and some of the daily challenges she faces in negotiations and contracts. She specifically discusses some of the key barriers within and beyond the legal language of CTAs and also shares highlights from her forthcoming book, The Four Villains of Clinical Trial Agreement Delays and How to Defeat Them.