Sahana R.

Regulatory Affairs is a passion for me more than profession. I have a Masters in Regulatory Affairs from University of Southern California, Los Angeles and Bachelor's in Biotechnology Engineering from RV College of Engineering. Internships with companies such as Philips Healthcare, Washington and Foundation Medicine, Cambridge moulded me for my full time jobs with RQMIS, Boston and CooperVision, Bay Area. Clinical research and Regulatory Affairs has always fascinated me. IQVIA and All of Us Research Clinical Trial program has strengthened my Clinical trial skills. Thanks to Biocon Academy - Keck Graduate Institute, Claremont collaboration program for giving me an exposure to Clinical Research and Regulatory Affairs in depth. I am currently working as a Senior Regulatory Affairs Consultant with easyQ Solutions. My main responsibilities here includes drafting TD, GSPR, Job aids and SOP's while working in accordance to the needs of the client. I mentor and manage junior team members (consulting/data and tech). I am looking forward to gain new Regulatory experience and strengthen my skills. My skills include the following : eQMS , VEEVA, Agile, ASANA, Lytho, VisionPack, M.Office