Biopharmaceutical β’ Biotechnology β’ Innovation β’ Research and Development β’ Manufacturing
November 19
πΊπΈ United States β Remote
ποΈ New Jersey β Remote
π΅ $195k - $371k / year
β° Full Time
π’ Junior
π‘ Mid-level
π¨ββοΈ Medical Director
π¦ H1B Visa Sponsor
Biopharmaceutical β’ Biotechnology β’ Innovation β’ Research and Development β’ Manufacturing
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.
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
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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