Company Description AbbVie'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 – immunology, oncology, neuroscience, and eye care – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on X, Facebook, Instagram, YouTube, LinkedIn and Tik Tok (https://www.tiktok.com/@abbvie) . Job Description Purpose: Support the planning and execution of the safety strategy for Immunology assets or potential assets in early development and during due diligence activities Main responsibilities In conjunction with the Executive Director, Translational Medicine, Immunology: + Supports the Safety Leads and Product Safety Teams (PSTs) to translate nonclinical and early clinical safety findings to facilitate benefit-risk decision making and risk mitigation in clinical development through phase 2a for AbbVie GI, dermatology and rheumatology development programs. + Reviews and/or summarizes scientific data for key safety documents (such as the Investigator’s Brochure or Development Safety Update Report) for early development assets to ensure they contain high quality medical safety content and are clearly written. + Facilitate scientific connections and interactions, info exchange across assets within the safety teams + Prepare material on competitive intelligence, current disease state and standard of care for key indications/ disease states + Supports PPS in assigned due diligence activities for immunology. + Compiles draft slide presentations for internal and external safety meetings as directed by Executive Director, Translational Medicine, Immunology + Interacts with and influences other cross functional departments (e.g. Toxicology, Pharmacokinetics, Business Development, Clinical and Regulatory Affairs), as needed, to ensure the successful development, design and implementation of comprehensive safety assessment to support study participants in early development programs. + Drives process improvement and change management for the Translational Medicine Immunology Safety team in conjunction with enterprise-wide and functional area plans. Qualifications + Scientific or clinical degree (e.g. NP/PA, PharmD, MS, PhD, MPH, including combinations) + 5+ years of experience in Pharmacovigilance / Clinical Development / Development biological Sciences experience in the pharmaceutical industry. + Expertise in translational science and/or early research in immune mechanisms of disease, as demonstrated, for example, through a peer reviewed publication record. + Experience participating in due diligence exercises to inform go/no-go decisions is strongly preferred. + Knowledge of clinical trial methodology, regulatory and compliance requirements governing clinical trials, and experience in development of clinical strategy and the design of study protocols + Ability to exercise judgment and address complex problems and create solutions across multiple projects + Must be able to lead and manage through influence. + Effectively provide input on technical safety documents + Strong ability to influence individual stakeholders and cross-functional teams in a collaborative environment + Must possess excellent oral and written English communication skills. + Ability to work effectively under circumstances of uncertainty and complexity. Additional Information Applicable only to applicants applying to a position in any location with pay disclosure requirements under state or local law: ​ ​ + The compensation range described below is the range of possible base pay compensation that the Company believes in good faith it will pay for this role at the time of this posting based on the job grade for this position. Individual compensation paid within this range will depend on many factors including geographic location, and we may ultimately pay more or less than the posted range. This range may be modified in the future.​ + We offer a comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) to eligible employees.​ + This job is eligible to participate in our short-term incentive programs. ​ + This job is eligible to participate in our long-term incentive programs​ ​ Note: No amount of pay is considered to be wages or compensation until such amount is earned, vested, and determinable. The amount and availability of any bonus, commission, incentive, benefits, or any other form of compensation and benefits that are allocable to a particular employee remains in the Company's sole and absolute discretion unless and until paid and may be modified at the Company’s sole and absolute discretion, consistent with applicable law. AbbVie is an equal opportunity employer and is committed to operating with integrity, driving innovation, transforming lives, serving our community and embracing diversity and inclusion. It is AbbVie’s policy to employ qualified persons of the greatest ability without discrimination against any employee or applicant for employment because of race, color, religion, national origin, age, sex (including pregnancy), physical or mental disability, medical condition, genetic information, gender identity or expression, sexual orientation, marital status, status as a protected veteran, or any other legally protected group status. US & Puerto Rico only - to learn more, visit https://www.abbvie.com/join-us/equal-employment-opportunity-employer.html US & Puerto Rico applicants seeking a reasonable accommodation, click here to learn more: https://www.abbvie.com/join-us/reasonable-accommodations.html Salary: $195,000 - $371,000