Senior Scientific Director, International Medical Affairs - Gastroenterology: Cross-IBD / Stand[...]

Job Description The Senior Scientific Director, International Medical Affairs provides specialist medical and scientific input into core strategic and operational medical affairs activities for the International Gastroenterology portfolio such as health‑care professional and provider interactions; generation of clinical and scientific data (enhancing therapeutic benefit and value); educational initiatives, scientific communications, value propositioning, and safeguarding patient safety (risk minimization activities and safety surveillance activities). As the Cross‑IBD and Standard of Care Lead, you will work closely with marketing and commercial teams to provide strategic medical input into strategies to elevate standard of care in IBD. Other key deliverables include leading evidence generation plans and tactics, driving scientific communication initiatives (both internal and external medical education, data, guidelines and value proposition), and owning the development and execution of critical medical education events requiring collaboration across multiple countries and affiliate sites. Position is based at our headquarters in Mettawa, IL following a hybrid schedule of 3 days/week onsite. Core Responsibilities Provides specialist medical insights and executes on data generation, communication, and expert engagement activities as deliverables to support relevant Asset Strategy Teams (ASTs) for late‑stage development program, including leading or contributing to comprehensive gap assessment, development of Scientific Communication Platform, and integrated evidence plans to support launch readiness. Leads external stakeholder interactions (Payers, Patients, Prescribers, and Providers). Drives GMA input into and influences the development of asset strategy in collaboration with International and BU Medical teams, Clinical Development, Commercial, Market Access, HEOR and other functional areas, providing leadership, oversight, and support for assigned indications/projects. Works closely with Brand Teams and relevant cross‑functional, area/affiliate medical teams to ensure appropriate pull‑through of prioritized medical activities. Provides relevant scientific and technical training to internal teams globally. Develops and maintains professional and credible relationships with key opinion leaders; actively participates in relevant Asset, cross‑functional teams and drives the development of medical affairs objectives aligned with strategy. Leads the development and execution of advisory boards focused on elevating standard of care, and collaboratively develops innovative research concepts for clinical data generation. Leads the development and execution of a standalone medical education event. Reviews, assesses and reports applicable Adverse Events (AEs) and Serious Adverse Events (SAEs) if assigned to AbbVie‑conducted clinical studies. Keeps abreast of professional information and technology through conferences and/or medical literature and acts as a specific therapeutic area resource. Initiates research projects and drives them to completion, resulting in high quality publications. Ensures budgets, timelines, compliance requirements are factored into programs' scientific activities. Qualifications Advanced Degree (PhD or PharmD). Additional post‑doctorate experience highly preferred. Typically 15 years’ experience in the pharmaceutical industry or equivalent. Minimum of 10 years of clinical trial or medical affairs experience in the pharmaceutical industry, academia, or equivalent. Proven leadership skills in a cross‑functional global team environment. Ability to interact externally and internally to support global business strategy. Expert knowledge in a relevant therapeutic specialty. Proven ability to run a clinical study or medical affairs cross‑functional team independently. Knowledge of clinical trial methodology, regulatory requirements governing clinical trials and experience in development strategy and the design of protocols. Must possess excellent oral and written English communication skills. People leadership experience required. Benefits Comprehensive package of benefits including paid time off (vacation, holidays, sick), medical/dental/vision insurance and 401(k) plan to eligible employees. Eligibility to participate in long‑term incentive programs. Equal Opportunity Statement AbbVie 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. #J-18808-Ljbffr