Associate Medical Director - Medical Safety Evaluation, Translational Medicine Immunology

2 days ago

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AbbVie

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Biopharmaceutical • Biotechnology • Innovation • Research and Development • Manufacturing

10,000+

Description

• 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. • Understand and apply pharmacology, chemistry and non-clinical toxicology to effectively conduct safety assessments. • Contribute to the authorship of key safety documents for early development assets. • Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents. • Analyze and interpret pre-clinical and clinical safety data and communicate the analysis and interpretation to cross-functional teams. • Conduct, summarize and communicate safety assessments in due diligence activities for Immunology.

Requirements

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

Benefits

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