Amrita S. - 20595 Medical Writer from Mississauga

● Master of Pharmacy qualified, regulatory and scientific content developer and currently has 5 years of experience as a medical writer. ● Skilled in authoring as well as quality checking of regulatory submission documents like clinical study reports, individual safety narratives, CTD modules; clinical trial participant documents like informed consent form. ● Experienced in regulatory medical writing; quality related writing, editing documents as per the company’s standards ● Have handled more than 10 top pharmaceutical clients such as Cipla, Glenmark, Astra Zeneca, Macleods, Pfizer, etc. ● Seeking to work with the most talented team of professionals in pharma/healthcare agency, ensuring career progression through constant guidance and confident about taking up newer job roles.