Kavitha S

Led a team in the Safety Review department, managing case allocations and ensuring adherence to client procedures. Responsible for performance evaluation and continuous improvement activities, while serving as a liaison between Accenture and the client team.

Managed the Safety Review process for non-serious cases, ensuring compliance with SOPs and effective resource utilization. Evaluated team performance and facilitated training and meetings to enhance team efficiency.

Coordinated and supervised various processes within the organization, focusing on improving policies and production efficiency. Liaised with senior management to develop and implement operational plans.

Processed and evaluated adverse event reports, ensuring accurate data entry and compliance with regulatory requirements. Collaborated with cross-functional teams on safety matters.

Worked in the Bio-Analytical department focusing on sample preparation and method development for pharmaceutical studies. Involved in US-FDA audits and ensured compliance with laboratory standards.

Grade: 85%

Activities and societies: Participated in various conferences and training sessions related to pharmaceutical sciences.

Studied Pharmaceutical Chemistry with a focus on the design, synthesis, characterization, and evaluation of mTOR inhibitors for anticancer activity. Achieved 85% in the program.

Grade: 74%

Activities and societies: Published research on novel CDK2 inhibitors and participated in various training and seminars.

Completed a Bachelor of Pharmacy focusing on the development of a spectrophotometric method for quantitation of Fexofenadine Hydrochloride and Pseudoephedrine Hydrochloride in pharmaceutical dosage forms. Achieved 74% in the program.