Anshul Thakral

Anshul Thakral

 
Anshul has over 20 years of experience in the pharmaceutical and biotech industries as a general manager, management consultant, commercial leader and entrepreneur. Most recently, he served as Chief Commercial Officer and EVP of Peri and Post-Approval Services at PPD. He started his career at PPD as Global Head of PPD Biotech and under his leadership PPD became a market leader for CRO services in the Biotech segment. Before PPD, Anshul ran the global life sciences business unit at Gerson Lehrman Group (GLG), where he created a customer business model to serve the pharmaceutical and biotechnology industries. Prior to GLG, he worked at McKinsey, where he was an associate principal in the health care practice. He currently serves on the boards of TriNetX, Saama Technologies, Orsini Specialty Pharmacy and Opthea Ltd. (observer).

Anshul earned his B.S and M.S.E in Biomedical Engineering from Johns Hopkins University and his MBA from the Wharton School at the University of Pennsylvania.

 

 

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Aaron Camp

Aaron Camp

 
Aaron has 18 years of experience in the pharmaceutical and biotech industries as a biostatistician. Most recently, Aaron served as Global Head of Biostatistics at ICON. At ICON, he managed a global team of 55 biostatisticians and provided statistical oversight for more than 100 oncology trials. Before ICON, Aaron worked as a biostatistician at PPD for 13 years with a focus on oncology and auto-immune therapeutic areas and an emphasis on program development and adaptive designs.

Aaron served in the US Army for 4 years and in the Texas National Guard for 4 years. He earned his B.S. in Mathematics from the University of Texas – San Antonio and his M.S. in Statistical Science from Southern Methodist University.
 

 

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James Cornwall, PhD

James Cornwall, PhD

 
James has close to 30 years professional experience in the pharmaceutical and CRO industries, working across a range of disciplines including academic research, clinical development, corporate development and investing. He works with the Abingworth investment team to source and evaluate new clinical co-development (CCD) investment opportunities and supports existing CCD investments.

Prior to joining Abingworth and Launch Therapeutics, James was Chief Business Officer at Nuvelution, a specialist CCD investment company. Before Nuvelution, he was with IQVIA as head of corporate development and regional board member for the Asia Pacific region, and previously with NovaQuest, Quintiles internal investment group, where he led multiple investments in Europe and the USA. James started his career in clinical research with positions of increasing responsibility at GSK, before moving to Quintiles in global operations and sales roles. He is a founder at Ninnion LLC and President US-Asia Pharma Advisory LLC.

James has a BSc in Pharmacology and a PhD in Neuropharmacology from the University of Bristol, UK, where he published over twenty peer reviewed papers. He completed postgraduate training in Executive Leadership, from the University of North Carolina Kenan Flagler Business School.
 

 

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Shao Chang, MD, PhD

Shao Chang, MD, PhD

 
Shao is a seasoned pharmaceutical executive with more than 15 years of experience. Most recently, Shao was Senior Vice President, Head of Clinical Development at BeiGene where he led a global team in three late-phase programs and six early-phase programs. Prior to BeiGene, Shao was Vice President, Global Medical Lead and Clinical Development Lead, Immuno-Oncology at AstraZeneca/MedImmune. Shao spent ten years at Eli Lilly as a Product Team Lead and Clinical Development Lead.

Shao earned his B.S. from Baylor University and completed his MD-PhD program at the University of Texas-Houston (McGovern Medical School). Shao’s hematology and research fellowships were completed at Washington University Medical School.
 

 

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Elisha Talley-Roithner

Elisha Talley-Roithner

 
Elisha has over 25 years of drug development experience. Elisha spent the last 14 years at PPD where she was most recently Head of Development Operations. In this role, she had global accountability for a $3.5B clinical trial portfolio. Elisha also led the team who developed and executed a COVID-19 vaccine program, achieving first time in man to emergency use authorization in less than 11 months. Elisha is recognized for generating and implementing innovative, strategic solutions. She is a founding member of PPD Biotech and led the creation and implementation of an industry-leading Biotech operating model which resulted in improved project cycle times and significant business expansion. Before PPD, Elisha led the Infectious Disease and Biotech project management teams at Covance (now Labcorp Drug Development).
 

 

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