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Collin Weller
VP, Product Management
Colin Weller has worked in the Drug Development industry for more than 20 years having spent large portions of time with Big Pharma and Biotech companies such as Pfizer, Amgen and AstraZeneca. Weller is driven by developing and deploying technology solutions into clinical research that enable an acceleration of the status quo timelines to ultimately bring therapies to patients faster.
Andrew MacKinnon
Executive General Manager, Customer Value
Mackinnon drives the development and application of eConsent for efficient, high-quality decentralized clinical trials. With 20 years of experience in clinical trial management across Pharma, Biotech, and CROs, he's committed to leveraging decentralized methodologies to ease clinical research burdens. Previously, he's held senior roles at Covance and focused on enhancing business performance.
Musaddiq Khan
VP, Customer Value - Digital Outcomes and TA Strategy
Musaddiq (“Muz”), with 18 years in clinical research, previously worked in clinical operations at PAREXEL, Roche, and AstraZeneca, and was the Director at Eli Lilly, leading Covid-19 Antibody program operations. Now, as Therapeutic Solutions Lead at Medable, he's dedicated to creating top-tier digital solutions for clinical research, enhancing operational delivery and innovation in the field.
Cindy Howry
VP eCOA
With over 35 years of experience, Howry is renowned for pioneering electronic data collection and clinical outcome assessments. With pivotal roles at assisTek, Arrowhead, and Bracket, she's significantly contributed to electronic data collection in clinical assessments. Cindy's academic background includes a Master's in Computer Science and a certification in Generative AI,
Jena Daniels
VP, Customer Value - Site and Patient Engagement
Jena, renowned for her work in digital clinical trials and recognized by PharmaVoice100 and as the Best Decentralized Clinical Trial Businesswoman of 2022, pioneered Medable's Patient Success department and Patient Caregiver Network. Daniels is dedicated to ensuring patients’ lived experiences inform the clinical trial experience.
Pam Tenaerts
Chief Scientific Officer
Dr. Tenaerts is one of the leading advocates for innovation in clinical trials, with a unique personal background as a clinical trials investigator, hospital research administrator and academic in both the U.S. and Europe. Dr. Tenaerts joins Medable from Duke, where she led CTTI’s efforts to develop and drive adoption of practices that increase the quality and efficiency of clinical trials.
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Medable unveils its new Partner Program, designed to empower contract research organizations (CROs) and other partners with generative AI-driven, self-service eCOA build capabilities for digitally enabled clinical trials.
Medable Introduces Long-Term Follow-Up Model for Cell & Gene Therapy (CGT) Trials to Reduce Costs and Improve Patient Access
Medable unveils its digital-first, Long-Term Follow-Up (LTFU) model for cell and gene therapy (CGT) trials. Medable’s platform reduces the burden on patients and sites involved in complex CGT trials and enhances scientific integrity with sustainable data capture across the FDA-required 15-year follow-up period for certain CGTs, including those using genome-editing techniques.
New Data Reveals DCT Components Linked to Improvements in Clinical Trial Access Among Underrepresented Communities
Medable's groundbreaking study with the Tufts PACT Consortium highlights the transformative impact of decentralized clinical trials (DCTs) on diversity.