Worldwide Clinical Trials
Mahwish Moghul possesses extensive experience in regulatory affairs, currently serving as Associate Director of Global Regulatory Affairs at Worldwide Clinical Trials since February 2014. Mahwish has held various roles at Worldwide Clinical Trials, including Senior Manager, Site Activation and Regulatory Lead, and Global Senior Regulatory Specialist. Prior experience includes serving as Global Study Start-up Manager for EMEA and Senior Regulatory Specialist at PharmaNet/i3 from October 2011 to October 2012, and earlier roles as Senior Regulatory Specialist and Senior Associate I in International Regulatory Affairs at Biogen Idec from August 2006 to July 2010.
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Worldwide Clinical Trials
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About Worldwide Clinical Trials Worldwide Clinical Trials is a leading full-service global contract research organization (CRO) that works in partnership with biotechnology and pharmaceutical companies to create customized solutions that advance new treatments. Our capabilities include bioanalytical laboratory services, Phase I-IV clinical trials, and post-approval and real-world evidence studies – all powered by our team members who bring their expertise and a collaborative, personalized approach to each clinical program. Anchored in our company’s scientific heritage, our dedicated therapeutic focus on cardiovascular, metabolic, neuroscience, oncology, and rare diseases, is applied to develop flexible plans and solve problems quickly for our customers. Our talented team of 3,000+ professionals spans 60+ countries, and embraces a culture of diversity, equity, inclusion, and belonging (DEI&B). We are united in cause with our customers to improve the lives of patients through new, innovative therapies. For more information on Worldwide, visit www.Worldwide.com.