Priyanka C

Experience

• 

  Tata Consultancy Services

  Sept 2022 - now

  Senior Process Associate

  Managing, preparing, and reviewing clinical documents for regulatory submissions, including drug safety aggregate reports such as NDA-AR, DSUR, PBRER, and ACO, ensuring compliance with regulatory standards. Authoring and performing quality checks of CTD modules such as m2.7, m2.5, and m5.To perform extensive literature search across medical literature databases such as PubMed and Research Gate.