Amanda Huff

Background

About Amanda Huff

Drug developer with 23+ years of research experience including - Program oversight of clinical assets in rare, genetic CNS diseases - Oversight of Phase I-IV international infectious disease, hepatology, and neurology study experience - Oversight of Phase cardiovascular and nephrology studies including dialysis studies - Oversight of pediatric infectious disease studies and programs - Budget and timeline development and management - Writing and updating IND submissions, protocols and amendments, Investigator’s Brochures, AE/SAE narratives, PIPS, pharmacokinetic summaries, interim safety and efficacy summaries- Clinical decision support software development Strong leadership and team-building skills with proven track record in managing internal and external resources, and collaborating with partners and cross-functional groups to project completion. Able to set realistic priorities, implement appropriate strategies, make informed decisions, and manage multiple projects. Capable of critical and strategic thinking to inform decisions and implement development plans.