SMID Biotech & Specialty Pharma

Adivo Associates is a global management consulting firm headquartered in San Francisco; Adivo specializes in biotech and pharma industry and serves top tier companies in the field.  Work on developing strategy and market analysis across the value chain for small biotech and global pharma in various therapeutic areas, with a special focus on autoimmune diseases and rare diseases. Leverage internal and external databases (claim database, IMS, MRB, etc.) to analyze market dynamics… Show more Adivo Associates is a global management consulting firm headquartered in San Francisco; Adivo specializes in biotech and pharma industry and serves top tier companies in the field.  Work on developing strategy and market analysis across the value chain for small biotech and global pharma in various therapeutic areas, with a special focus on autoimmune diseases and rare diseases. Leverage internal and external databases (claim database, IMS, MRB, etc.) to analyze market dynamics and facilitate strategic decisions on market entry, pipeline strategy optimization, and marketing activities. Execute secondary researches (sell-side reports, literature, corporate reports, etc.) and interview KOLs to gain insight into competitive landscapes, product adoption, regulatory, and market assessment. Responsible for project management and liaising with global team members to compose PowerPoint presentations. Held an internal education session on topics regarding the Chinese healthcare market. Show less

ForDoz Pharma is an early-stage specialty pharmaceutical company. Involved in the early-stage drug development of two liposomal drugs, including formulation optimization and method developments. Completed verification and validation for developed methods and instruments according to ICH and FDA guidelines; attended FDA training programs on 505(j) filing and injectable drug development. Established the cGMP lab in the company with other team members and drafted Standard… Show more ForDoz Pharma is an early-stage specialty pharmaceutical company. Involved in the early-stage drug development of two liposomal drugs, including formulation optimization and method developments. Completed verification and validation for developed methods and instruments according to ICH and FDA guidelines; attended FDA training programs on 505(j) filing and injectable drug development. Established the cGMP lab in the company with other team members and drafted Standard Operating Procedures (SOPs). Show less

 Responsible for projects that are backing preclinical/clinical trials for cutting-edge drugs; the results supported to progress into the next stages of clinical development. Prepared results and documents for FDA review on behalf of clients, leveraging the knowledge of FDA regulations and new drug development process.