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.
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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.
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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.
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Spectraforce Technologies
Jul 29, 2025