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Senior Manager, Us Medical Review

3+ years
$113,821.60 to $170,732.40
10 April 24, 2025
Job Description
Job Type: Full Time Education: PharmD/MD/PhD Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Job Title: Senior Manager, US Medical Review
Location: Boston, Massachusetts, United States
Job ID: R-224452
Date posted: 14/04/2025


About the Company:

Alexion, AstraZeneca Rare Disease, is a global biopharmaceutical company focused on the development and commercialization of life-changing medicines for patients with rare diseases.


Job Responsibilities:

  • Medical and Scientific Review:

    • Provide medical and scientific expertise to support the development of high-quality promotional and medical materials, internal training materials, and communications as part of the Promotional Review Committee (PRC) and Medical Review Committee (MRC)

    • Maintain broad, in-depth knowledge of pathophysiology, pharmacotherapy, and clinical outcomes associated with assigned Alexion products and disease states

  • Metrics and Analytics:

    • Support the generation of therapeutic area metrics and analytics to aid in load management and forecasting future resources

  • Internal Training & Presentations:

    • Assist in the development and delivery of presentations to internal colleagues, including medical information inquiry metrics, customer insights, and training on medical information procedures

    • Potentially create content for Medical Affairs or review and fact-check data points for promotional materials

  • Product Complaints & Operational Initiatives:

    • Report any product quality complaints and adverse events to Quality Assurance/Drug Safety per corporate policies

    • Assist in the development and maintenance of SOPs, training modules, and database/system enhancements

    • Support broader activities in Medical Communications, including Medical Education and Scientific Communication


Required Qualifications:

  • Education:

    • Advanced scientific degree in pharmacy (PharmD) or related science (PhD, MD)

  • Experience:

    • 3 years of medical information or medical communications experience in the pharmaceutical/biotech industry

    • Proven success in negotiating and influencing stakeholders

    • Understanding of drug development, US (FDA) and global (EMEA) regulations, and pharmacovigilance reporting requirements

    • Strong written and verbal communication skills

    • Proficiency in literature searching and Microsoft Office Suite

  • Skills:

    • Excellent organizational, time management, and prioritization skills

    • Attention to detail and self-motivation


Preferred Qualifications:

  • Experience:

    • Experience providing medical review as part of an MLR team

    • Experience working with promotional/medical review systems (e.g., Veeva PromoMats)

    • Experience creating medical affairs content

    • Training or past experience in therapeutic areas such as rare disease, immunology, nephrology, hematology, oncology, neurology, or enzyme-replacement therapies

    • Experience working on product launches

    • Completion of a post-PharmD Fellowship in the pharmaceutical/biotech industry


Compensation and Benefits:

  • Salary:

    • Annual base salary ranges from $113,821.60 to $170,732.40

    • Overtime pay, short-term incentive bonus opportunity, equity-based long-term incentive program (salaried roles), and more

  • Benefits:

    • Qualified retirement program (401(k) plan), paid vacation and holidays, health benefits (medical, prescription drug, dental, and vision coverage), and more