Job Title: Medical Reviewer / Safety Reviewer Duration: 1 year to start Purpose: The Medical Reviewer has a key role within the designated Therapeutic Area. Working under the leadership of the Scientific Director / Medical Director , this role supports the development and execution of the therapeutic area medical strategy. Responsibilities include: Providing scientific, strategic, and operational input into core medical affairs activities (thought leader engagement, field provider interactions, clinical/scientific data dissemination). Supporting provider and payer educational initiatives and promotional material generation . Ensuring tactical execution is relevant to the market - physicians, patients, and payors . Primary Responsibilities: Medical Review for label, clinical data, and disease state. Provides subject matter expertise for commercial teams, including competitive assessments and scientific literature reviews. Aligns medical education and scientific initiatives with the Scientific Communication Platform . Top 3-5 Skills & Experience (in priority): Ability to work independently and quickly onboard. Experience performing medical review of medical and promotional materials. Experience reviewing in Veeva PromoMats and/or MedComms (CRM knowledge). Experience in AML or multiple therapeutic areas with proven adaptability in mastering new disease states. Ability to clearly communicate rationale for review decisions to Commercial & Medical teams. ? Qualifications: Scientific degree ; advanced degree ( MS, PhD, MD/DO, PharmD, NP, MSN ) preferred. 3-5 years of clinical, scientific/research, or industry-related experience with demonstrated leadership in a global matrixed environment. Strong understanding of legal & regulatory guidelines (OPDP, CDER/CBER, FDA CFR, ISO, PhRMA code, ICH, GCP, HIPAA, EU Directive). Experience in Medical Affairs principles , study design, publications, and clinical trial methodology. Strong interpersonal & communication skills to interact internally & externally for global business strategy. Ability to influence without direct reporting relationships in a team/matrix environment. ? Responsibilities: Contribute to therapeutic area strategy development and execution. Lead medical education tactics , advisory boards, and thought leader engagement. Plan and execute conferences , representing AbbVie at external meetings (investigator meetings, scientific associations, etc.). Conduct Medical Review (MR) training for label, clinical data, and disease state. Manage budgets for assigned projects , including vendor management. Support clinical/scientific data generation (e.g., IIS strategy). Provide competitive assessments & literature reviews for commercial teams. Align educational/scientific initiatives with the Scientific Communication Platform . Contribute to Medical Information (MI) content and training on MI materials. Support launch readiness planning . #J-18808-Ljbffr Davita Inc.
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