Lead the launch of Infigratinib for achondroplasia.
Build territory plans to meet and exceed sales goals.
Partner with providers and families to improve patient access.
Engage geneticists, pediatric endocrinologists, and orthopedic teams.
Ensure compliant, clinically relevant discussions with HCPs.
Collaborate with Field Medical, Reimbursement, and Marketing for launch success.

🎯 Requirements

8–10 years in pharma/biotech; 4+ years in rare disease.
Achondroplasia or pediatric rare disease experience preferred.
BS/BA required; MBA a plus.
Willingness to travel extensively.
Strong account management and territory planning skills.
Deep clinical acumen and market knowledge in skeletal dysplasia.

🎁 Benefits

Market-competitive compensation and equity
401(k) with employer match
Health, dental, vision benefits for you and dependents
Hybrid work model with flexible schedule
Generous PTO and holidays
Career development programs and learning resources

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