Director, Medical Science Liaison

🕒 March 18

🐎 Kentucky, North Carolina, +4 more states – Remote

🐎 Kentucky – Remote 🌲 North Carolina – Remote 🌴 South Carolina – Remote 🎸 Tennessee – Remote ⚔️ Virginia – Remote ⛰️ West Virginia – Remote

💵 $230k - $275k / year

⏰ Full Time

🔴 Lead

👔 Director

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Celcuity

WebsiteLinkedInAll Job Openings

51 - 200 employees

🧬 Biotechnology

💊 Pharmaceuticals

🔥 Funding within the last year

💰 $500M Post-IPO Debt - Celcuity on 2025-09

Biotechnology • Pharmaceuticals

Celcuity is a clinical-stage biotechnology company developing targeted therapies that comprehensively block the PI3K/AKT/mTOR (PAM) pathway to treat multiple solid tumors. Its lead product candidate, gedatolisib, is a potential first-in-class pan-PI3K and mTORC1/2 inhibitor in late-stage clinical development (including Phase 3 VIKTORIA trials) for HR+/HER2- advanced breast cancer and other indications such as prostate cancer. The company advances a focused pipeline of PAM pathway inhibitors, publishes clinical data, engages with investors and regulators, and is mission-driven to improve outcomes for cancer patients.

📋 Description

• Identify and cultivate professional relationships KOLs in designated tumor types. • Maintain cross-functional field partnerships allowing for appropriate collaboration with field commercial teams (sales, market access, etc.), and Clinical Development associates. • Maintain and develop synergistic relationships with KOLs to expand research, advisory, and educational partnership opportunities. • Assist the Clinical Development Team in the identification and education of potential clinical trial sites, assist, upon request, in troubleshooting issues during clinical trial conduct. • Develop scientific expertise on all Celcuity’s products, related disease states, and the clinical practice for a given therapeutic area. • Communicate scientific content, written and verbal, related to Celcuity’s products and related disease states. • Be knowledgeable of and follow all applicable laws, SOPs and guidance documents ensuring compliance • Provide scientific training to internal colleagues. • Participate in the Medical, Legal, and Regulatory review process, as needed, in the role of scientific expert. • Identify, categorize, and communicate key clinical insights related to assigned disease state and products. • Other duties as assigned.

🎯 Requirements

• MD, PharmD, or PhD in Life Sciences, D.Sc., D.N.P, or D.O. degree • Solid tumor oncology experience • Excellent presentation and communication skills • Conveying complex scientific concepts and information appropriately tailored to the audience (internal staff, physicians, nurses, patient advocacy groups, formulary committees, etc.) • 3+ years of related pharmaceutical Medical Science Liaison experience • Breast Cancer experience • Knowledge of clinical research design and GCP in the oncology area • Experiences at small / start-up biopharmaceutical company • Strong business acumen • Experience with payor groups, market access teams, formulary committees, and treatment guidelines • Experience managing territory resources and budgets. Demonstrated self-starter • Experience launching products

🏖️ Benefits

• Medical insurance • Dental insurance • Vision insurance • 401(k) match • PTO • Paid holidays • Annual performance incentive bonus • New hire equity package