Senior Manager, US Medical Review Meta+

This is what you will do:

The Senior Manager US Medical Review will sustain and promote Alexions professional standing and integrity amongst patients health care professionals and the pharmaceutical / biotech industry by providing high quality Medical Review of all material used by the Commercial and Medical teams. This role is responsible for developing and maintaining current broad and in-depth knowledge of pathophysiology pharmacotherapy and patient outcomes associated with assigned Alexion products and disease states.

As necessary this individual may support broader activities in Medical Communications including Medical Education and Scientific Communications.

The employee carries out this role in accordance with departmental SOPs corporate policy and other legal and regulatory requirements.

You will be responsible for:

• Will provide essential medical and scientific expertise review advisement and oversight to support 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).

• Developing and maintaining current broad and in-depth knowledge of pathophysiology pharmacotherapy and clinical outcomes associated with assigned Alexion products and disease states.

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

• Assisting in the development and delivery of various presentations to internal colleagues (e.g. medical information inquiry metrics and customer insights; training of commercial and medical field teams on medical information procedures; medical booth training at medical congresses)

• As applicable potentially creating content for Medical Affairs and/or assisting in the review fact-checking of data points assessment of appropriateness of references cited in materials submitted to the Promotional and Medical Review Committees

• As applicable reporting any product quality complaints and adverse events to Quality Assurance / Drug Safety per corporate policies.

• As applicable supporting various operational initiatives including development and maintenance of SOPs; training modules; database/system enhancements; vendor oversight; etc.

• As applicable providing support to broader activities in Medical Communications including Medical Education and Scientific Communication.

You will need to have:

• Advanced scientific degree in pharmacy (PharmD) or related science (PhD MD) required with 3 years of medical information or medical communications experience in the pharmaceutical/biotech industry.

• Demonstrated success in negotiating and influencing stakeholders.

• Understanding of drug development US (FDA)and global (e.g. EMEA) regulations and reporting requirement for reporting pharmacovigilance events and product quality complaints

• Strong written and verbal communication skills

• Proficiency in literature searching skills.

• Proficiency with Microsoft Office Suite

• Attention to detail.

• Self-motivation to drive for results.

• Excellent organizational time management and prioritization skills

• The duties of this role are generally conducted in an office environment. As is typical of an office-based role employees must be able with or without an accommodation to: use a computer; engage in communications via phone video and electronic messaging; engage in problem solving and non-linear thought analysis and dialogue; collaborate with others; maintain general availability during standard business hours.

We would prefer for you to have:

• Experience providing medical review as part of an MLR team.

• 3-years of relevant experience in academia and/or pharmaceutical/biotech industry. Or 2-years of relevant experience in pharmaceutical/biotech industry.

• Prior experience working with promotional/medical review systems (e.g. Veeva PromoMats)

• Experience creating medical affairs content.

• Adept at learning new software / applications

• Training or past experience in assigned therapeutic area(s) or rare disease immunology nephrology hematology oncology neurology enzyme-replacement therapies.

• Experience working on product launches.

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

The annual base salary (or hourly rate of compensation) for this position ranges from $113821.60 to $170732.40. Hourly and salaried non-exempt employees will also be paid overtime pay when working qualifying overtime pay offered may vary depending on multiple individualized factors including market location job-related knowledge skills and experience. In addition our positions offer a short-term incentive bonus opportunity; eligibility to participate in our equity-based long-term incentive program (salaried roles)to receive a retirement contribution (hourly roles) and commission payment eligibility (sales roles). Benefits offered included a qualified retirement program 401(k) plan; paid vacation and holidays; paid leaves; and health benefits including medical prescription drug dental and vision coverage in accordance with the terms and conditions of the applicable plans. Additional details of participation in these benefit plans will be provided if an employee receives an offer of employment. If hired employee will be in an at-will position and the Company reserves the right to modify base salary (as well as any other discretionary payment or compensation program) at any time including for reasons related to individual performance Company or individual department/team performance and market factors.

Date Posted

30-May-2025

Closing Date

04-Jun-2025Alexion is proud to be an Equal Employment Opportunity and Affirmative Action employer. We are committed to fostering a culture of belonging where every single person can belong because of their uniqueness. The Company will not make decisions about employment training compensation promotion and other terms and conditions of employment based on race color religion creed or lack thereof sex sexual orientation age ancestry national origin ethnicity citizenship status marital status pregnancy (including childbirth breastfeeding or related medical conditions) parental status (including adoption or surrogacy) military status protected veteran status disability medical condition gender identity or expression genetic information mental illness or other characteristics protected by law. Alexion provides reasonable accommodations to meet the needs of candidates and employees. To begin an interactive dialogue with Alexion regarding an accommodation please contact Alexion participates in E-Verify.