Associate Director, Us Medical Affairs & Evidence Generation Training
Argenx
Remote, US
Remote
Us medical affairs and evidence generation
Field medical and internal medical stakeholders
Scientific excellence and field readiness
Argenx is seeking an Associate Director for US Medical Affairs & Evidence Generation Training, a remote position focused on developing and executing training programs for the Medical Affairs team. The ideal candidate will have a strong background in Medical Affairs within the biotech or pharmaceutical industry, and the role emphasizes collaboration, innovation, and scientific excellence
Job Summary
The Associate Director, Training, US Medical Affairs & Evidence Generation is responsible for supporting the strategy, planning, and execution of training programs for the US Medical Affairs and Evidence Generation organization.
This role partners closely with Medical Affairs leadership, Medical Directors, MSL Leadership, and cross-functional partners to ensure training programs drive scientific excellence, field readiness, and continuous capability development.
Key attributes include being a proactive learner, detail-oriented, having a growth mindset, humility, high emotional intelligence, and being collaborative.
Matching Summary
Match Score: 85
Argenx is seeking an Associate Director for US Medical Affairs & Evidence Generation Training, a remote position focused on developing and executing training programs for the Medical Affairs team. The ideal candidate will have a strong background in Medical Affairs within the biotech or pharmaceutical industry, and the role emphasizes collaboration, innovation, and scientific excellence.
Skills & Requirements
Must-have
US Medical Affairs and Evidence Generation
Field medical and internal medical stakeholders
Scientific excellence and field readiness
Adult learning principles and innovative methodologies
Nice-to-have
Proactive learner and growth mindset
High emotional intelligence and collaborative
Experience in neurology or immunology
Key Requirements
Advanced degree (PhD, PharmD, MD)
5+ years biopharmaceutical, clinical, or post-graduate experience
3+ years of Medical Affairs field or in-house experience
Demonstrated experience executing training programs for field medical or internal medical teams
Experience with Medical, Regulatory, and Legal review process