On-Demand Webinar

View this on-demand cardiovascular webinar to hear Worldwide experts discuss:

  • Emerging heart failure therapies & trial designs
  • Demonstrating value when novelty is not enough
  • Diverse stakeholders - the who, what & why? 

Access the on-demand webinar today! 

Michael Murphy, M.D., Ph.D.
Chief Medical & Scientific Officer

Dr. Murphy’s professional career has spanned over 25 years in positions within the pharmaceutical industry. He is board-certified in psychiatry and has a doctorate in pharmacology, with training at Tulane University, Stanford University and the Mt. Sinai School of Medicine. His contributions as Chief Medical & Scientific Officer at Worldwide encompass all therapeutic areas under Worldwide’s umbrella, and include translational research activities, scientific regulatory support, and protocol development for phases I–IV. He has been a consultant for the Duke Clinical Research Institute and is Founder and Research & Development Editor for American Health and Drug Benefits™. As a lecturer within the Center for Experimental Pharmacology and Therapeutics, Harvard-MIT Division of Health Sciences and Technology (HST) for 17 years, Dr. Murphy contributed to the curriculum for a two-year Clinical Investigator Training Program.

Toni Bransford, M.D., FACC, FASE
Senior Medical Director, Medical & Scientific Affairs

Toni spent 10 years in academia as a clinical cardiologist at St. Louis University followed by University of Minnesota. Her subspecialty being cardiac imaging, she spent several years performing industry sponsored research in ultrasound microbubble imaging at St. Louis University and investigator-initiated research at University of Minnesota. She was a fixture in the cardiology clinics as well and was noted as one of the top cardiologists in St. Louis in 2000. In 2006 she left academics to work in the pharmaceutical industry, primarily big pharma where she has worked for 10 years (Schering Plough, Novartis). She has worked for Worldwide Clinical Trials since August, 2015 in the cardiovascular therapeutic area as a medical monitor.

LORNA GRAHAM
Associate Director, Project Management, Evidence

Lorna Graham has 17 years clinical research experience. Lorna has worked in both the pharmaceutical and CRO industry in various roles including data management, site management and worked across therapeutic areas including cardiovascular, CNS, oncology, tropical disease and women’s health. Lorna has over 10 years’ experience in project management, which includes study and Late Phase senior project management. Lorna’s Late phase experience includes; Effectiveness evaluation studies, risk management plans, risk evaluations and mitigation strategies, disease registries, observational non interventional studies, healthcare provider surveys and contributions to a global economic dossier for a HIV compound.
JOSIE MEASURES
Vice President Biostatistical Operations

Josie has over 25 years’ experience as a medical statistician. She started her career analyzing nutritional surveys at the Ministry of Agriculture, Fisheries and Food. She them moved to the Medical Research Council providing expert statistical support to clinical researchers. Josie has spent the majority of her career in the pharmaceutical industry at Pfizer and Quintiles before joining Worldwide Clinical Trials in 2014. Josie specializes in developing high performing Biostatistical Operations and enjoys working closely with teams to develop efficient and effective clinical trials. Josie has an MSc in Biometry and an MBA (with distinction).

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