Clinical Pharmacologist

• Provide subject matter expertise in the design, conduct, and reporting of clinical trials
• Contribute to clinical pharmacology sections of clinical study protocols, study analysis plans, clinical study reports and clinical development plans
• Lead clinical pharmacology studies and perform PK and PK/PD analyses (e.g., NCA analysis)
• Preparation of standalone PK/PD reports or PK/PD section of Clinical Study Report (CSR)
• Collaborate with biostatistician, clinical operation, bioanalytical scientist and clinician for the execution and management of Phase I-III studies
• Present PK findings and represent clinical pharmacology in cross-functional study team settings

• PhD degree or equivalent in Pharmaceutics, Pharmacology, Pharmacokinetics or PharmD
• 1-2 years of industry or equivalent experience and working knowledge of analysis software (e.g., WinNonlin, Phoenix NLME and NONMEM) preferred
• Ability to translate pharmacokinetic findings into potential clinical impact is highly desirable

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.