Senior Medical Director, Immunology, Global Patient Safety

Compensation: USD 182,000 - USD 346,000 - yearly About Abb Vie Abb Vie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience - and products and services in our Allergan Aesthetics portfolio. For more information about Abb Vie, please visit us at www.abbvie.com. Follow @abbvie on Linked In, Facebook, Instagram, X and You Tube. Responsible for supporting the Product Safety Leads (PST) and potentially support one or more products as the PST Lead under the direction of the Therapeutic Area (TA) Lead and Global TA Head in ensuring safety in one or more products to through surveillance, signal detection, validation and assessment. Interpreting regulations related to pharmacovigilance supporting all patient safety activities.

Responsibilities: Understanding and application of the pharmacology, chemistry and non-clinical toxicology to effectively conduct safety surveillance Safety surveillance for pharmaceutical / biological / drug –device combined products Contribute to the authorship of key pharmacovigilance documents, including but not limited to, medical safety assessments, regulatory responses and risk management plans Apply current regulatory guidance as appropriate for safety surveillance and authorship of PV documents Analyze and interpret aggregate safety data and communicate these analysis and interpretation to cross-functional teams Ability to effectively write, review and provide input on technical documents Lead the strategy for periodic reports (PSUR’s, PADER’s etc.)Oversight of safety surveillance and pharmacovigilance activities for products in clinical trials and post marketing Lead and implement risk management strategy for assigned productsMD / DO with 2+ years of residency with patient management experience and Master Public Health is preferred in addition to MD / DO but not required 2 – 4 years of Pharmacovigilance experience in the pharmaceutical industry Effectively analyze and guide analysis of clinical data and epidemiological information Effectively present recommendation / opinions in group environment Write, review and provide input on technical documents Self-starting and can work independently Work collaboratively and lead cross-functional teams Applicable only to applicants applying to a position in any location with pay disclosure requirements under state orlocal law: The compensation range described below is the range of possible base pay compensation that the Companybelieves ingood faith it will pay for this role at the timeof this posting based on the job grade for this position. Individualcompensation paid within this range will depend on many factors including geographic location, andwemayultimatelypaymore or less than the posted range. This range may bemodifiedin thefuture.paid time off (vacation, holidays, sick)medical/dental/vision insurance 401(k) to eligible employees This job is eligible toparticipatein our long-term incentiveprograms.

Note: No amount of payis considered to bewages or compensation until such amount is earned, vested, anddeterminable. The amount and availability of any bonus, commission, incentive, benefits, or any other form ofcompensation and benefitsthat are allocable to a particular employeeremainsin the Company's sole andabsolutediscretion unless and until paid andmay bemodifiedat the Company’s sole and absolute discretion, consistent withapplicable law. Abb Vie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives and serving our community. Equal Opportunity Employer/Veterans/Disabled.