Senior Principal Biostatistician – Epidemiology

Edwards Lifesciences

Senior Principal Biostatistician leading clinical trial designs, collaborations for innovative solutions at Edwards Lifesciences. Responsible for statistical leadership in clinical research and partnerships.

Posted 7/30/2026full-timeRemote • California • 🇺🇸 United StatesSenior💰 $151,000 - $215,000 per yearWebsite

Core Competencies

Role fit

Core Competencies

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Demonstrates expertise in Biostatistics, including the design and analysis of clinical trials and observational studies, while effectively communicating statistical findings and economic models to stakeholders. Proven ability to lead cross-functional teams, mentor junior staff, and manage projects within regulatory frameworks.

Highest-signal resume keywords

Expertise In SASOutcomes Research MethodologiesClinical Trial DesignStatistical ModelingRegulatory Guidelines Knowledge

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills

Statistical AnalysisEconomic ModelingData AnalysisObservational Study DesignCausal InferenceEpidemiologyStatistical MethodologyBudget ManagementVendor ManagementClinical Trial Analysis

Soft Skills

LeadershipCommunication SkillsInterpersonal SkillsProblem-SolvingOrganizational Skills

Tools & Technologies

SASRS-PlusMS Office Suite

Industry Keywords

Real-World EvidenceBiostatistics Standard Operating ProceduresGood Clinical PracticeInternational Council for HarmonisationFood and Drug AdministrationISO Standards

Tech Stack

Tools & technologies

Google Cloud Platform

About the role

Key responsibilities & impact

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

What you’ll need

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

Comp & perks

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