Rakesh Chugh, Md Email & Phone Number

Total Experience – 18+ years (15 years in Pharma/CRO/Medical writing and 3 years in academia) MD in Clinical Pharmacology from Delhi University and over 18 years experience in clinical development of drugs in neurology, CNS, antibacterials, and biosimilars and the conduct and implementation of phase I, II and III clinical trials and medical writing including clinical and safety reports, narratives, and medical letters; Special focus on Portfolio Project Management.Involved in multiple face-to-face and telephonic interactions with International Regulatory Agencies including FDA, EMA, CFDA, and DCGI for discussion on Clinical Development Plans and Protocols of New Chemical EntitiesExperienced in designing (protocol and clinical development plans) as well as leading multicenter, global clinical trials in the United States, India, and Europe, with experience in the Sponsor as well as CRO settings.Primary expertise has been in the areas of CNS, biosimilars, antibacterials, neurology, pain, diabetes, and specialized review of ophthalmology data from clinical trials. I have led project teams to successful end-to-end completion of phase I (including specialized clinical pharmacology studies), II, III global clinical trials by functioning as the lead Project Director for Sponsor Pharmaceuticals as well as serving as the primary representative/face of the CRO to global pharmaceuticals and providing strong leadership, proactive project management, and good communication links. Experienced as a speaker at global investigators’ meetings and conferences, and training workshops with relevant national and international publications.Specialties: MD Pharmacology, Project Management, Clinical Development

Listed skills include Vendor Management, Strategy, Clinical Pharmacology, Therapeutic Areas, and 16 others.

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  Lady Hardinge Medical College, Delhi University

  Pharmacology