Sarita T.

Sarita T. has a comprehensive work experience in the pharmaceutical industry. Sarita is currently serving as the Director of GVP Quality Assurance at Taiho Oncology, Inc. since July 2021.

Prior to their current position, Sarita worked at Alvogen for 7 years, starting in April 2014 as the Vice President of Global Pharmacovigilance & Drug Safety. During their time at Alvogen, they led project integration teams for pharmacovigilance and quality complaint projects during mergers. Sarita also played a key role in the migration of safety databases and configuration of global legacy products, while implementing new workflows that resulted in a 30% personnel synergy.

Before joining Alvogen, Sarita held various positions at Actavis. From 2005 to 2014, they served as the Director of Pharmacovigilance Operations. Prior to that, they were a Senior Manager of Pharmacovigilance at Actavis (Alpharma) from 2003 to 2005 and a Manager of Drug Safety at Actavis (Purepac) from 2001 to 2003.

Sarita'scareer in the pharmaceutical industry began in 1998 at Roche, where they worked as a Drug Safety Specialist until 2001.

With their extensive experience and expertise in pharmacovigilance and drug safety, Sarita T. has made significant contributions to the industry.

Sarita T. pursued a Doctor of Pharmacy (PharmD) degree at Shenandoah University. The dates of enrollment and completion are not specified. No further educational experiences or degrees were mentioned.