Investigator– DMPK, Mechanistic ADME
Location:
, Pennsylvania
Posted:
September 18, 2017
Reference:
WD115181
Basic qualifications:
• PhD degree in medicinal chemistry, pharmaceutical sciences, or related areas with strong knowledge of drug transporters and pharmacokinetics.
• Sufficient level of expertise of transporters and/or drug metabolizing enzymes and the role they play in drug disposition and safety.
• Good knowledge of mechanistic understanding for drug-drug interaction (DDI) and ability to predict DDI risk using in silico tools as well as physiologically-based pharmacokinetic (PBPK) model simulation (simCYP or other platforms).

Preferred qualifications:
• Pharmaceutical industry working experience, knowledge in HIV therapeutic area as additional strength.
• Deep expertise in in vitro- in vivo extrapolation, DDI risk assessment at different drug development phases, and/or strong PBPK modeling skills.
• Working experience in pre-clinical drug development environment, in-depth understanding of drug ADME mechanism and translation of safety risks to the clinic.
• Track record of scientific achievement.
• Demonstrated ability to work effectively in a team environment and across departments and good communication and writing skills.

Details:
Provide expertise and recommendations to project representatives and/or project teams to support optimal delivery of mechanistic ADME data and to ensure patient's safety by sufficient risk assessment towards drug transporter characterization, metabolic pathways and DDI prediction

Key Responsibilities:
• Responsible for supporting DMPK project representatives and/or project teams to deliver ADME data and to provide risk assessment towards drug biotransformation, transporters and DDI, especially for projects and/or programs in HIV therapeutic area.
• Responsible for coaching junior scientists to execute studies in in vitro ADME studies, DDI risk assessment, and to trouble shoot experimental issues.
• Responsible for delivering high quality study reports, publications, and regulatory dossiers to support drug development.

*LI-GSK

Contact information:

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