Celcuity
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.
Senior Manager – Statistical Programming
Job not on LinkedIn
🕒 March 30
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Celcuity
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
• Provide technical expertise and oversight of programming by CRO partners • Work as part of a multidisciplinary team, providing programming support for clinical trials • Coordinate and execute on preparation, execution, reporting and documentation of statistical programming activities • Design and develop SAS programs to execute statistical analysis and clinical trial reporting deliverables • Develop and perform appropriate quality control and validate clinical trials outputs • Establish collaborative partnerships with internal and external programmers, data managers, and clinical staff
🎯 Requirements
• Minimum 8 to 12 years of industry experience (pharmaceuticals, biotechnology, or CRO) • Strong CRO oversight experience • Solid verbal and written communication skills • Demonstrated ability to speak up appropriately and ask necessary questions • Experience in clinical trials related to oncology for solid tumors • Experienced hands-on skill in programming with SAS is required • Good knowledge of statistics and oncology drug development process • Strong experience performing quality control of datasets (ADaM, SDTM, SEND) based on CDISC dataset specifications
🏖️ Benefits
• Annual performance incentive bonus • New hire equity package • Medical insurance • Dental insurance • Vision insurance • 401(k) match • Paid time off • Paid holidays
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