Senior Principal Biostatistician – Epidemiology

🕒 July 30

🏄 California – Remote

🏄 California – Remote

💵 $151k - $215k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

🦅 H1B Visa Sponsor

This company has sponsored H1B visas in the past.

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Edwards Lifesciences

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1958

🏥 Healthcare

💼 Consulting

🍽️ Food & Beverage

Healthcare • Consulting • Food & Beverage

Edwards Lifesciences is a global leader in patient-focused medical innovations. The company specializes in heart valve disease solutions, offering products and services such as transcatheter heart valves and mitral and tricuspid technologies, as well as surgical heart valve solutions. Edwards Lifesciences also focuses on critical care technologies including hemodynamic monitoring, remote monitoring, and predictive monitoring. The company conducts clinical research and is committed to improving patient lives through innovative cardiovascular disease solutions, while being a responsible corporate citizen with an emphasis on global corporate giving.

📋 Description

• Lead end-to-end evidence strategies, designing observational studies, interventional trials, and real-world evidence (RWE) programs to support pipeline and on-market products • Build economic models (cost-effectiveness, budget impact) to clearly communicate the clinical, and economic value of Edwards products • Statistical lead on multiple clinical trials, lead the coordination of analyses for study report and other documents and provide programming and validation support of these analyses • Collaborate with cross-functional partners and external analysts in the execution of studies and implementation of field-based, customer-focused initiatives and partnerships (e.g., models, presentations, publications, formulary/regulatory dossiers). • Represent Biostatistics on multiple project/study teams and coordinate/communicate with management and other team members regarding project/study status and timeline update • Provide statistical expertise and guidance to internal and external stakeholders on ad hoc data analysis requests and publication/presentation efforts related to the project team • Research and recommend novel statistical methodology and/or approaches • Contribute to the improvement, standardization, and globalization of Biostatistics processes and procedures, including the development of Biostatistics Standard Operating Procedures (SOPs) and Work Instruction Manuals (WIMs) • Lead the efforts of data analysis for data monitoring committee as needed • Mentor junior statisticians and work with management in resource allocation and budget/timeline development activities

🎯 Requirements

• Bachelor's Degree in Statistics, Biostatistics, or related field • 8 years of previous analytical experience in clinical trials or Master's Degree or equivalent in Statistics, Biostatistics, or related field, 7 years of previous analytical experience in clinical trials or Ph.D. or equivalent in Statistics, Biostatistics, or related field , 4 years of experience • Deep knowledge of outcomes research and RWE methodologies (study design, statistics, data sources, and implementation) • Deep knowledge of observational study methods, causal inference, economic model (cost-effectiveness), epidemiology • Proven experience managing vendors, budgets, and building productive partnerships with internal stakeholders and external experts/KOLs • Demonstrated leadership in matrixed environments, including the ability to direct work across functions to deliver shared objectives • Proven expertise in SAS required; experience using other software packages (e.g., R, S-Plus) preferred • Proven expertise in MS Office Suite including Word, PowerPoint, Access, and Excel • Excellent written and verbal communication skills and interpersonal relationship skills including negotiating and relationship management skills with ability to drive achievement of objectives • Keeps abreast of new developments in statistics and regulatory guidance • Expert understanding and knowledge in statistical methodologies related to clinical trial designs, statistical modeling and data analyses • Expert understanding and knowledge of regulatory guidelines (e.g., GCP, ICH, FDA, ISO) relevant to in Pharmaceutical/Medical Device research setting • Excellent problem-solving, organizational, analytical and critical thinking skills • Strong leadership skills and ability to influence change • Ability to provide training and coaching to lower level employees • Experience in facilitating change, including collaboration with management and executive stakeholders

🏖️ Benefits

• Competitive salaries • Performance-based incentives • Wide variety of benefits programs to address diverse individual needs