I have about 12+ years of working experience in clinical research in key roles as medical, regulatory and safety expert for various regulatory submissions such as FDA, EMA and DCGI in all therapeutic areas predominantly oncology and biosimilars. I have a close rapport with KOLs and subject experts in various therapeutic areas. Till now I have been part of more than 70+ studies in different phases of drug development. Possess good communication & leadership skills, extensive monitoring experience, sound knowledge of clinical research & global regulatory requirements.
I like to take new challenges and succeed with determination and focused approach. In my journey as an intrapreneur, I have successfully implemented medical services and pharmacovigilance processes in my current organization and now look forward to fly on global horizon by exploring exciting opportunities.
Medical Monitoring, Medical Writing, Regulatory Affairs, Pharmacovigilance,
Project Management, Translational medicine, Life cycle Management
Strategies, New Product Selection, NCE & NDDS Development, Biosimilars,
Vaccines, Medical Devices, Software Development, Training and team development, Technical Branding
Hardworking, Intelligent, Agile,