Career Summary Pharmacist by education, with 10 years of Industrial Experience in various domains of Preclinical and Clinical Research and Development as well as IMP Supply Chain Management. R&D Professional with 4 years of Clinical Research experience from within the CRO as well as Sponsor environment that includes PK/PD studies, Phase II, III and IV studies and more than 1 year of experience in Preclinical research laboratory. 5 years of experience in IMP Supply Chain Management under Global set-up. Worked for 3 months at Novartis, Switzerland location. Key experiences are in Clinical Trial Process Development, Clinical Trials related Regulatory Affairs, Handling Quality Issues, Project Management, Drug Supply Management, Internal & External Stakeholder Management and Employee training/mentoring. Actively participated in rolling out various quality processes & procedures in the current and past organizations. Area of Interest Drug Development related Project Management Supply Chain Management Clinical Research and Regulatory Affairs

Highlights:

• Clinical Research
• Clinical Supply
• Trial Management
• Microsoft
• Microsoft Excel
• Microsoft Office
• Microsoft Word
• Microsoft Word
• Clinical Research
• Management
• Research
• Analytical Skills
• Audit
• Cardiovascular
• Compliance
• ENT