
501 - 1000 employees
Founded 2004
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.
🕒 June 26
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501 - 1000 employees
Founded 2004
🏥 Healthcare
💼 Consulting
📦 Logistics
Healthcare • Consulting • Logistics
Everest Clinical Research is a global contract research organization (CRO) that provides end-to-end clinical trial services and biometrics expertise to pharmaceutical and biotechnology sponsors. The company offers clinical operations and project management, risk-based quality management and centralized monitoring, medical monitoring, pharmacovigilance, clinical data management, biostatistics and statistical programming, regulatory strategy and submissions, and technology solutions such as IRT/RTSM and ePRO/eCOA. Everest positions itself as a high-touch, quality-driven partner with global reach and therapeutic expertise across oncology, neurology, respiratory, rare diseases and immunology.
• Manage clinical trial programs/projects from one or multiple clients • Provide day to day technical and operational leadership to project teams • Provide statistical oversight on projects in the assigned drug development programs/projects • Ensure sound statistical methodologies in study design, sample size estimation, statistical analysis planning, and reporting • Coach, mentor, develop, and provide technical review and advice to less experienced Biostatisticians and Statistical Programmers • Participate in the writing of trial protocols and research proposals • Review and provide input to clinical data management deliverables • Write Statistical Analysis Plans, Statistical Reports • Perform overall Quality Control review on statistical deliverables • Ensure compliance with relevant regulatory requirements • Interact with regulatory agencies and support sponsor in new drug applications
• Ph.D. degree in statistical science, mathematical analysis or related fields with at least 7 years of relevant experience • Master’s degree in these fields with at least 10 years of relevant experience • demonstrated exceptional ability and performance
• medical, dental, and vision coverage • life & AD&D insurance • short- and long-term disability • tuition reimbursement • fitness reimbursement • employee assistance program (EAP) • 401(k) retirement / pension plan • generous paid time off and sick leave • performance based bonus
Apply Now🕒 June 24
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