Director, Medical Science Liaison, North Central

Location: North Central (Minnesota, Iowa, Nebraska, South Dakota, North Dakota, Kansas, Missouri) This region does not include Illinois, but the prospective new hire can reside in the Chicagoland area.

Position Summary:

We are seeking a Director, MSL who will report to the Senior Director, Western US Field Medical. The Director, MSL will be responsible for scientific exchange with Health Care Providers (HCPs) and key decision makers (managed care, payers, formulary committees, etc.) on Celcuity’s products, relevant disease states, and in support of clinical trials.

MSL’s combine a strong business acumen, disease state knowledge, clinical knowledge/experience, market awareness, and serve as a conduit for Celcuity’s scientific data to external customers while providing external market and clinical insights internally to cross-functional teams. Travel within the territory and the US for medical conferences will be expected.

Responsibilities:

• 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.

Qualifications:

• 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

About Us:

Celcuity is a publicly traded commercial-stage biotechnology company developing targeted therapies for multiple solid tumor indications. The company's first FDA-approved product is REVTORPYK (gedatolisib), targets all class I isoforms of PI3K and the mTOR complexes to comprehensively block the PAM pathway. The PAM pathway is an important signaling pathway involved in many cancers and has historically been challenging to target.

A Phase 3 clinical trial, VIKTORIA-1, evaluating gedatolisib in combination with fulvestrant with or without palbociclib in patients with HR+/HER2- locally advanced or metastatic breast cancer (“ABC”), supported FDA approval of REVTORPYK for use in patients without a PIK3CA mutation detected. Gedatolisib phase 3 clinical development programs are focused on the treatment of patients with HR+/HER2- ABC in the 1L and 2L settings. A Phase 1b/2 clinical trial evaluating gedatolisib in combination with darolutamide in patients with metastatic castration resistant prostate cancer, is on-going.

Celcuity is an Equal-Opportunity Employer:

Celcuity is committed to fair and equitable compensation practices, and we strive to provide employees with total compensation packages that are competitive. For this role, the anticipated base pay range is $230,000-$256,000 DOE. The exact base pay offered for this role will depend on various factors, including but not limited to the candidate’s geography, qualifications, skills, and experience.

The successful candidate will be eligible for an annual performance incentive bonus and a new hire equity package. Celcuity also offers various benefits offerings, including, but not limited to, medical, dental, vision insurance, 401(k) match, PTO, and paid holidays.

Notice to Recruiters/Staffing Agencies:

Recruiters and staffing agencies should not contact Celcuity through this page. All recruitment vendors (search firms, recruitment agencies, and staffing companies) are prohibited from contacting our hiring manager(s), executive team members, or employees directly.

We require that all recruiters and staffing agencies have a fully executed, formal written agreement on file. Celcuity’s receipt or acceptance of an unsolicited resume submitted by a vendor organization to this website or employee does not constitute an actual or implied contract between Celcuity and such organization and will be considered unsolicited. Celcuity will not be responsible for related fees.