Celcuity is a clinical-stage, publicly traded biotechnology company headquartered in Minneapolis that focuses on extending the lives of cancer patients through targeted therapies for solid tumors. Its flagship product, gedatolisib, is an intravenously administered, first-in-class PI3K/AKT/mTOR pathway inhibitor with a unique mechanism of action and differentiated pharmacokinetics compared to existing PI3K or mTOR therapies. The company is advancing gedatolisib in Phase 3 trials for hormone-receptor positive/HER2-negative advanced breast cancer in both first- and second-line settings, while also evaluating a combination with darolutamide in metastatic castration-resistant prostate cancer. Celcuity's distinctive approach lies in its comprehensive targeting of cellular drivers of tumor growth, positioning it at the forefront of innovative, multi-pathway cancer therapeutics.
Open Positions
Senior Manager, Regulatory Affairs, CMC
8+ years of Regulatory Affairs experience, Bachelor's degree in a science or health-related field, Excellent command of GXPs
Associate Director, Medical Writing
D., PharmD, MD/DVM, degree in biological science preferred with a minimum of 5 years of experience in oncology regulatory medical writing (MS with a minimum of 10 years relevant experience)
Director, Biostatistics
10+ years of clinical trials experience with at least 3 years in oncology clinical trials. Master's degree in statistics, biostatistics or a closely related field; PhD preferred
Vice President, Commercial Operations
15+ years of experience in biopharma Commercial/Business operations, experience in building-out business operations infrastructure, and strong people management skills
Senior Director, Scientific Strategy and Communications
PhD or other advanced degree, 5+ years of oncology experience, 10+ years in pharma/biotech company
Director, Medical Science Liaison, New England
3+ years of related pharmaceutical Medical Science Liaison experience, Breast Cancer experience, Knowledge of clinical research design and GCP in the oncology area
Senior Manager, Statistical Programming
Minimum 5-10 years of industry experience in developing or overseeing efficient development of submission-ready programming code for clinical trials using the SAS-based Statistical Computing Environment
Associate Director, Clinical Science
Advanced Science/Clinical Degree, 3 or more years clinical trial experience, Oncology research experience preferred
Vice President, Drug Safety & Pharmacovigilance
3+ years of clinical experience, 10+ years of pharmacovigilance or drug safety experience, 5+ years of senior leadership experience
Director, Medical Science Liaison, North Central US
MD, PharmD, or PhD in Life Sciences, solid tumor oncology experience, 3+ years of related pharmaceutical Medical Science Liaison experience
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