A member of the Crinetics Pharmaceuticals ClinPharm team since 2022 with over 10 years of clinical pharmacology and product development experience to the team performing data analyses as well as providing the input into protocol statistical analysis plan design and study reports. Prior experiences include completion of the UNC/Quintiles PKPD fellowship, as well as experience in pharmaceutical product development performing PK/PD analyses for a wide variety of products and indications as a part of Medimmune’s Clinical Pharmacology team and later in the Clinical Pharmacology group at PPD, development of alternative tobacco products at Altria Client Services and building a small start-up global CRO. Extensive experience with BE/BA studies, single and multiple ascending-dose studies and double-blind study designs. Additional tasks include departmental and study budget coordination, project management for standalone TK/PK studies for internal and external clients, and database design utilizing CDISC and ADaM standards.Specialties: Data analysis, programing, protocol development and study coordinating
Listed skills include Pharmacokinetics, Clinical Development, Clinical Trials, Oncology, and 9 others.