Medical Writing Associate I Full-time Job

Together, we’re on a mission to make good health more affordable and accessible, to help millions around the world enjoy healthier lives. It’s a mission that bonds our people across nearly 60 countries and a rich, diverse variety of nationalities and backgrounds. Working here means working with the world’s leading manufacturer of generic medicines, and the proud producer of many of the products on the World Health Organization’s Essential Medicines List. Today, at least 200 million people around the world take one of our medicines every single day. An amazing number, but we’re always looking for new ways to continue making a difference, and new people to make a difference with.

How you’ll spend your day Literature search, preparation of Clinical study protocols and PSP according to required day to day Guidelines and Regulatory Requirements by using Product Monographs/Prescribing Information/Summary of Product Characteristics etc., as applicable. Preparation of Informed Consent Form/s (ICF) in line with Clinical study protocol. MedDRA and WHO-DD coding of clinical studies Preparation/review of Case Record Forms (CRF). System improvements as basis.