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argenx SE

Senior Manager, US Medical Promotional Review

argenx SE, Baltimore, Maryland, United States

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Senior Manager, US Medical Promotional Review page is loaded## Senior Manager, US Medical Promotional Reviewlocations:

United States - Remotetime type:

Full timeposted on:

Posted Todayjob requisition id:

REQ-3792*Join us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multi-dimensional expansion to reach more patients through a rich pipeline of differentiated assets, led by VYVGART, our first-in-class neonatal Fc receptor blocker approved for the treatment of gMG, and with the potential to treat patients across dozens of severe autoimmune diseases.**We are building a new kind of biotech company, one that maintains its roots as a science-based start-up and pushes our commitment to innovate across all corners of our business. We strive to inspire and grow our company, our partnerships, our science, and our people, because when we do, we deliver more for patients.*The Sr. Manager, US Medical Review, will be responsible for the medical review of promotional materials to ensure to ensure statements are scientifically valid and accurate, truthful and not misleading. This includes providing solutions-oriented feedback and working collaboratively within the Medical Review Community.**ROLES & RESPONSIBILITIES**



Serve as the Medical Reviewer for scientific accuracy in the US Materials Committee (MRC).



Provide independent medical review to ensure statements are scientifically valid and accurate, truthful and not misleading, including the appropriateness of references cited.



Communicate and collaborate effectively with Medical Review Community to cultivate a positive relationship



Serve as Librarian for reference evaluation for us in the US Material Review Committee (MRC)



Maintain scientific knowledge, including: labeling, associated therapeutic areas, relevant literature, treatment guidelines and competitor information, through ongoing internal and external data sources (e.g., training, conferences)**SKILLS AND COMPETENCIES**



Able to partner with Medical Review Community stakeholders and embrace cross-sub-team working within Medical Review



Ability to critically evaluate literature, interpret complex data, write effectively, articulate information to a variety of audiences, and negotiate with counterparts from cross-functional areas



Must be a strong team player with a positive attitude and demonstrate flexibility to plan and prioritize in a dynamic environment



Ensures the highest degree of quality and medical accuracy for all outputs developed



Completes all work in accordance with regulatory requirements, industry standards, and argenx policies**REQUIREMENTS**



Doctorate Degree (PharmD/MD/PhD)



2-4 years biopharmaceutical industry in medical affairs leading the review of marketing and/or scientific communications



Experience in content management systems (Veeva Vault or similar) is preferred



Strong scientific/medical written and verbal communication skills required*At argenx, all applicants are welcomed in an inclusive environment. They will receive equal consideration for employment without discrimination on the basis of race, color, religion, sex, sexual orientation, gender identity, national origin, protected veteran status, disability, or any other applicable legally protected characteristics. argenx is proud to be an equal opportunity employer.**Before you submit your application, CV or any other personal details to us, please review our* *to learn more about how argenx B.V. and its affiliates (“argenx”) will handle and protect your personal data. If you have any questions or you wish to exercise your privacy rights, please contact our Global Privacy Office by email at* *privacy@argenx.com**.**If you require reasonable accommodation in completing your application, interviewing, or otherwise participating in the candidate selection process please contact us at hr.us@argenx.com. Only inquiries related to an accommodation request will receive a response.* #J-18808-Ljbffr