bala sudhakar mandarapu

Bala Sudhakar Mandarapu has a diverse work experience spanning multiple industries. bala sudhakar started their career at GSK as a Medical Business Associate, where they played a key role in the business development of products like Augmentin and Arixtra. bala sudhakar'sresponsibilities included managing distribution channels, conducting market research, and market segmentation.

bala sudhakar then joined Sanofi Pharmaceuticals as a Senior Executive, leading a team for product Depura in Chennai. bala sudhakar successfully converted a significant number of healthcare professionals to use their product.

At AbbVie, Bala worked as a Validation Analyst. bala sudhakar collaborated closely with users to develop user requirements for Trackwise and participated in technical impact assessment meetings for the development of functional requirements. bala sudhakar also developed IQ/OQ/PQ test scripts within HP Quality Center for validation purposes.

Currently, Bala is working at RxAdvance as an Operations and Implementation Analyst. bala sudhakar is involved in various analyses and strategic projects related to pharmacy benefit management (PBM) implementation. This includes working on aspects such as group hierarchy, enrollment, eligibility, benefits, and formulary. Bala also configures plan benefits and performs claim testing to ensure accurate claim adjudication. bala sudhakar collaborates with business and clinical stakeholders to ensure requirements are met and coded to specifications.

Overall, Bala Sudhakar Mandarapu has gained significant experience in operations, analysis, implementation, validation, business development, and team leadership throughout their career.

Bala Sudhakar Mandarapu obtained their Bachelor's degree in Pharmaceutical Sciences from Bapatla College of Pharmacy in 2012. bala sudhakar later pursued a Master's degree in Project Management from Northeastern University, which they completed in 2017. In addition to their formal education, Bala Sudhakar Mandarapu also obtained certifications in "Introduction to FDA Drug Review and Approval Process" from the FDA and "Protecting Human Research Participants" from the NIH Clinical Center. The specific months for obtaining these certifications are not provided.