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You will be updated with latest job alerts via emailJoin us as we transform immunology and deliver medicines that help autoimmune patients get their lives back. argenx is preparing for multidimensional expansion to reach more patients through a rich pipeline of differentiated assets led by VYVGART our firstinclass 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 sciencebased startup 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.
Our MSLs are a fieldbased extension of the Medical team who represent and reflect argenxs values as a sciencedriven patientcentric organization. They engage with key stakeholders at academic and community health centers serve as a strategic partner to fellow cross functional team members and are experts on argenxs scientific data products and trials. MSLs report to the Head Immunology & Payer Medical Science Liaisons.
Roles and Responsibilities:
Developing medical and scientific expertise in immunology pipeline indications
Develop and maintain the highest scientific and medical expertise of relevant diseases
Compounds development indications and treatment plans
Be acknowledged internally and externally as an expert
Partner with HEOR Patient Advocacy andGlobal Commercial Planning and Readiness to create a thorough internal understanding of pipeline indication opportunities
Identify potential highimpact medical research projects and publication opportunities (e.g. white papersto inform treatment guidelines) in line with argenx identified areas of interest
Attend appropriate local national and international meetings and congresses to gather intelligencedevelop productive collaborations ensuring insights are shared within argenx
HCP engagement
Identify recommend and support site principal investigators (PIs) for ongoing and planned clinical trials
Promote clinical trial engagement through scientific exchange and presentations
Ensure timely and informative scientific/medical exchanges and education for healthcare communityon topics like disease awareness diagnostics treatment and adherence that accurately reflect scientificdata and research objectives compliantly and in line with medical strategy
Respond to questions from the healthcare community with integrity compliance andadherence to all legal regulatory and argenx guidelines policies & procedure
Responsible for tailoring engagement strategies by adeptly recognizing and accommodating thestakeholder archetypes (e.g. academic vs community) and their unique informational needs
KOL engagement
Develop and maintain relationships with healthcare KeyOpinion Leaders (KOLs) to collaborate on researchprojects advisory boards and peertopeer educational initiatives
Engage in development related activities by collaborating with PI and study sites to facilitateparticipation in clinical trials and provide guidance on study protocols patient recruitment etc.
Collaborate with KOLs on evidence generation appropriately including sponsored translational and outcomes research
Crossfunctional collaboration
Ensure close working relationship with crossfunctional field partners Global Commercial Planning and Readiness team Clinical Development/Operations compliantly to ensure launch readiness
Support crossfunctional teams to ensure operations are patientfocused including rapidly responding tointernal and external requests to discuss specific situations and challenges and provide medical affairssupport to all stakeholders
Skills and Competencies:
Crosstherapeutic area portfoliooriented mindset and strong aptitude foreffectively working with crossfunctional teams
Scientific and customercentric mindset with successful trackrecord of delivering results that meet or exceed targetedobjectives
Demonstrated ability to build relationships and collaborateproductively with external stakeholders (e.g. medical expertshealthcare professionals)
Effective collaborator on crossfunctional teams with a varietytechnical expertise and backgrounds
Able to quickly understand complex disease areas treatmentsand clinical development plans
Thorough understanding of clinical trial phases and
Able to problem solve proactively and translate territory /organizational needs into action
Can operate with significant autonomy to assess priorities andcustomize decisions in real time
Flexible to travel within region USA and global based on business needs
Education Experience and Qualifications:
Scientific healthcare or medical degree (PharmD PhD MD DO)
3 years fieldbased experience in biopharmaceutical industry
Preferred candidate is located in Boston New York or Philadelphia (plus surrounding locations)
Therapeutic area experience in rheumatologyimmunology and/or other rare diseases is an advantage
Preference to candidates with experience working with clinical research organizations (internal or as partners) to impact clinical trial
Strong clinical scientific and healthcare business acumen
Strong knowledge of the US healthcare landscape including hospitalsystems and healthcare professionals
Strong understanding of compliance legal and regulatorylandscape related to interactions with healthcare professionals
Fluency in translating market research and datadriven insightsinto actionable strategic initiatives
Proficient in Microsoft Office Suite and VEEVA
#LIHybrid
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 . Only inquiries related to an accommodation request will receive a response.
Full-Time