RESPONSIBILITIES

• In this role, you will lead design of clinical pharmacology studies as well as analysis, interpretation, and reporting of PK, drug disposition, and drug metabolism data from clinical studies for compounds and biologicals in therapeutic areas of immunology and oncology utilizing state of the art technology in support of clinical development plans.
• You will perform PK and PK/PD modeling, contribute to PK related regulatory documents and draft PK sections in support of clinical development plans, and provide PK perspective on cross functional teams.
• You will also participate in regulatory interactions as needed as well as evaluate feasibility of clinical studies and provide input to the design and review of clinical protocols.
• In addition, you must maintain a high proficiency on the latest scientific literature in the areas of drug metabolism, PK, PK/PD and clinical pharmacology.
• You will also serve as a mentor to junior level PK scientists

REQUIREMENTS

• A PhD or a PharmD with a postdoctoral fellowship training in PK, Biopharmaceutics or a related field with a minimum of three years experience in PK, PK/PD and drug metabolism techniques industry experience is preferred.
• Experience in designing, conducting and interpreting studies in PK, population PK, PK/PD correlations, modeling and simulation utilizing state of the art applications is highly desirable.
• Candidate must display strong written and oral communication skills necessary to deliver scientific presentations.
• The ability to work in a dynamic team oriented environment as demonstrated by participating in and contributing to cross functional teams is necessary.
• Experience in building an internal network of collaborators is desired.

HOW TO APPLY