Argenx
Associate Director, Medical Affairs Content Development
Argenx, Boston, Massachusetts, us, 02298
Associate Director- Medical Affairs Content Development
Find out more about this role by reading the information below, then apply to be considered.The Associate Director -Medical Affairs Content Development will lead the content creation, and maintenance, of materials for the Neuromuscular Therapeutic Area within the US Medical Affairs and Evidence Generation Community. This is a highly visible role within the Neuromuscular Therapeutic Area, and the individual work in close partnership with Medical Directors, MSL Directors, MSLs, and Medical Training, to develop strategically-aligned Medical Affairs content for use across a range of external and internal stakeholders.ROLES AND RESPONSIBILITIESEnsures all Medical materials are relevant, scientifically accurate, and consistent with cited appropriate scientific literature, internal scientific information, and company values and standardsHelps identify digital innovation to support content development, access, and delivery including enhanced scientific engagement via remote channelsEnsure all appropriate stakeholders are involved in the development, review and approval of materials.Lead development of scientifically accurate, fair balanced slide decks for field medical teams based on strategic direction and field team needs, while utilizing expertise of other argenx functionsResponsible for the localization of materials for the US affiliate while ensuring the information is aligned with local labellingManages materials through the US medical, legal and regulatory review processEnsure the highest degree of quality and medical accuracy for all outputs developedComplete all work in accordance with regulatory requirements, industry standards, and argenx policiesExhibits broad knowledge of assigned therapeutics areas, product labelling and regulatory guidanceServes as medial affairs liaison to cross-functional groups for the incorporation of current medical/scientific information into department documents and processesSKILLS AND COMPETENCIESAble to effectively network and partner with internal and external stakeholders and embrace cross-functional workingStrong operational capabilities, eye for detail and commitment to advance and adhere to processesDemonstrated project management experienceUnderstand and demonstrate the importance of providing superior customer service to all clients to support the businessExcellent communication skills: verbal, written and when giving presentationsAble to thrive as part of a team and when working independentlyProven track record of delivering results that meet or exceed targeted objectivesDetailed understanding of industry regulations and practices relating to medical affairsEDUCATION, EXPERIENCE AND QUALIFICATIONSAdvanced degree (MD, PhD, PharmD or equivalent) in a scientific discipline3+ years industry experience, working within Medical Affairs preferred.Experience managing vendors for content creationExperience in componentized content creation is preferredExperience in content management systems similar to Veeva Vault is preferredSignificant experience in pharmaceutical or biomedical writing and communications, including group facilitation and presentation to diverse audiencesJoin 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.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.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.PDN-9c805e97-2da5-43e8-baff-0ad36a309fcb
Find out more about this role by reading the information below, then apply to be considered.The Associate Director -Medical Affairs Content Development will lead the content creation, and maintenance, of materials for the Neuromuscular Therapeutic Area within the US Medical Affairs and Evidence Generation Community. This is a highly visible role within the Neuromuscular Therapeutic Area, and the individual work in close partnership with Medical Directors, MSL Directors, MSLs, and Medical Training, to develop strategically-aligned Medical Affairs content for use across a range of external and internal stakeholders.ROLES AND RESPONSIBILITIESEnsures all Medical materials are relevant, scientifically accurate, and consistent with cited appropriate scientific literature, internal scientific information, and company values and standardsHelps identify digital innovation to support content development, access, and delivery including enhanced scientific engagement via remote channelsEnsure all appropriate stakeholders are involved in the development, review and approval of materials.Lead development of scientifically accurate, fair balanced slide decks for field medical teams based on strategic direction and field team needs, while utilizing expertise of other argenx functionsResponsible for the localization of materials for the US affiliate while ensuring the information is aligned with local labellingManages materials through the US medical, legal and regulatory review processEnsure the highest degree of quality and medical accuracy for all outputs developedComplete all work in accordance with regulatory requirements, industry standards, and argenx policiesExhibits broad knowledge of assigned therapeutics areas, product labelling and regulatory guidanceServes as medial affairs liaison to cross-functional groups for the incorporation of current medical/scientific information into department documents and processesSKILLS AND COMPETENCIESAble to effectively network and partner with internal and external stakeholders and embrace cross-functional workingStrong operational capabilities, eye for detail and commitment to advance and adhere to processesDemonstrated project management experienceUnderstand and demonstrate the importance of providing superior customer service to all clients to support the businessExcellent communication skills: verbal, written and when giving presentationsAble to thrive as part of a team and when working independentlyProven track record of delivering results that meet or exceed targeted objectivesDetailed understanding of industry regulations and practices relating to medical affairsEDUCATION, EXPERIENCE AND QUALIFICATIONSAdvanced degree (MD, PhD, PharmD or equivalent) in a scientific discipline3+ years industry experience, working within Medical Affairs preferred.Experience managing vendors for content creationExperience in componentized content creation is preferredExperience in content management systems similar to Veeva Vault is preferredSignificant experience in pharmaceutical or biomedical writing and communications, including group facilitation and presentation to diverse audiencesJoin 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.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.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.PDN-9c805e97-2da5-43e8-baff-0ad36a309fcb