Overview:
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.
Responsibilities:
* Perform PK and PK/PD analyses (e.g., NCA analysis);
* Works closely with Clinical Pharmacologist in the preparation of PK Analysis Plan, PK/PD reports or PK/PD section within the Clinical Study Report (CSR);
* Collaborate with Biostatistician, Clinical Operations, Bioanalytical Scientist, and the Medical team for the execution and management of Phase I-III studies; and
* Present PK findings and represent Clinical Pharmacology in cross-functional study team settings.
Qualifications:
* Master's degree in Pharmaceutics, Pharmacology, Pharmacokinetics or related area,
* 1-2 years of industry experience preferred but not required
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