Develop and execute territory plans for skeletal dysplasia teams to meet sales goals.
Demonstrate product knowledge of Infigratinib and achondroplasia to HCPs.
Partner with Field Medical Directors and HUB to maximize customer and family satisfaction.
Build relationships with KOLs and advocacy groups to expand awareness.

🎯 Requirements

8-10 years in pharma/biotech; 4+ years in rare disease.
BS/BA required; MBA a plus.
Willingness to travel extensively.
Proven product/indication launch experience.
Account management and cross-functional collaboration skills.
Strong clinical acumen and stakeholder education.

🎁 Benefits

401(k) with employer match
100% employer-paid medical, dental, and vision
Flexible PTO and paid holidays
Hybrid work model with in-office days
Fertility and family-forming benefits
Career development programs

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