Associate Medical Director - Medical Safety Evaluation, Translational Medicine Immunology

November 19

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AbbVie

Biopharmaceutical β€’ Biotechnology β€’ Innovation β€’ Research and Development β€’ Manufacturing

Description

β€’ Responsible for supporting Product Safety Leads (PSTs) to translate nonclinical and early clinical safety findings, facilitate benefit-risk decision making and risk mitigation for one or more developmental products and during due diligence activities. β€’ Understand and apply pharmacology, chemistry and non-clinical toxicology to effectively conduct safety assessments. β€’ Contribute to the authorship of key safety documents for early development assets. β€’ Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents. β€’ Analyze and interpret pre-clinical and clinical safety data and communicate the analysis and interpretation to cross-functional teams. β€’ Conduct, summarize and communicate safety assessments in due diligence activities for Immunology.

Requirements

β€’ MD / DO with 2+ years of residency with patient management experience (required) β€’ Expertise in translational science and/or early research in immune mechanisms of disease, as demonstrated through a peer reviewed publication (preferred) β€’ Effectively analyze pre-clinical and clinical data (required) β€’ Background in bench or clinical research is a plus β€’ Effectively write technical documents with direction β€’ Work collaboratively in a team environment and be self-starting and able to work independently β€’ Ability to effectively present recommendation / opinions in a group environment β€’ Fluency, both written and oral, in English

Benefits

β€’ Paid time off (vacation, holidays, sick) β€’ Medical/dental/vision insurance β€’ 401(k) eligibility β€’ Short-term incentive programs β€’ Long-term incentive programs

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