Jobs at Cytel

Supports epidemiology and real-world evidence studies by preparing claims and EHR data, developing analytical databases, programming statistical analyses, creating algorithms, linking datasets, and producing tables, figures, reports, and presentations. Partners with epidemiologists, statisticians, vendors, clients, and internal stakeholders across Medical Affairs, Patient Safety, Risk Management, and Clinical Development. Requires expertise in SQL, SAS or R, RWE data sources, applied statistics, and project management.

Leads portfolio strategy, solution architecture, commercial growth, and delivery alignment for complex life sciences services. Partners with business development, marketing, sales, and functional experts to shape opportunities, design scalable offerings, support proposals, and improve profitability. Oversees portfolio governance, client outcomes, forecasting, scope management, and sales-to-delivery handoffs. Represents the organization with strategic clients and through industry thought leadership.

Provides technical and functional leadership for epidemiological and real-world evidence statistical programming. Leads hands-on development and validation of SAS and R programs, analysis datasets, tables, figures, and reproducible workflows using healthcare data. Mentors programmers, oversees internal and CRO deliverables, establishes standards and quality processes, supports regulatory and scientific outputs, and collaborates with epidemiologists, statisticians, and data scientists across projects and therapeutic areas.

Supports epidemiology and real-world evidence studies by preparing claims and EHR data, developing analytical databases, conducting statistical analyses, and producing tables, figures, reports, and presentations. The role assists with protocols and analysis plans, coordinates with data vendors and stakeholders, applies regression and survival methods, and supports Medical Affairs, Patient Safety, Risk Management, and Clinical Development initiatives. Strong SQL, SAS, or R expertise and experience with pharma RWE analytics are required.

Lead or support Phase I-IV clinical trial programming using SAS and CDISC standards to generate and validate SDTM/ADaM datasets, TLFs, and submission documents. Perform production and QC/validation programming, complex ad-hoc reports, and efficacy analyses while coordinating with cross-functional teams and serving as study lead when required.

Lead statistical activities for Phase I-IV clinical trials from protocol design through reporting. Represent statistics on cross-functional teams, oversee programmers/CROs, perform QC and inferential analyses using SAS/R, apply statistical, machine learning and deep learning methods for modeling/simulation, and mentor junior statisticians.

Lead statistical activities for Phase I-IV clinical trials from protocol design through reporting. Provide statistical oversight, collaborate cross-functionally, supervise programmers/CROs, apply SAS/R and ML/DL methods for analyses and automation, and support regulatory, safety, and publication deliverables.

Lead statistical activities for Phase I-IV clinical trials from protocol design through reporting. Represent statistics on cross-functional teams, oversee programming/CRO work, perform QC, inferential analyses, modeling/simulation, and apply machine learning/deep learning to generate actionable insights. Mentor junior statisticians and support safety, publications, and regulatory responses.

Lead statistical design and analysis for Phase I-IV clinical studies, develop protocols and SAPs, perform efficacy and exploratory analyses, run simulations, apply advanced methods (mixed models, longitudinal), oversee datasets (ADaM/CDISC), use R and SAS for analyses, and provide strategic statistical guidance to cross-functional teams supporting regulatory submissions.

Designs and delivers R-based data and analysis infrastructure for clinical trials. Develops reusable R packages, visualizations, tools, and documentation; partners with study teams and leads training and change management.

Provide project-level financial analysis, forecasting, and executive reporting. Translate financial data into recommendations, support ad hoc modeling and strategic initiatives, and develop project finance best practices and dashboards.

Lead statistical activities for clinical trials from protocol design through reporting. Provide statistical oversight, collaborate with cross-functional teams and CROs, apply SAS/R (and ML) for analyses, automate processes, and mentor junior statisticians.

Lead strategic statistical consulting engagements, design innovative statistical and clinical development solutions, build client relationships, grow business, mentor consulting teams, represent Cytel externally, and travel regularly to engage senior stakeholders.

The Senior Director, Business Development will drive Cytel’s Pharma client relationships, create strategic sales plans, and oversee client-focused initiatives to expand business growth.

Lead territory revenue growth by managing full sales cycle, building long-term client relationships, evangelizing Cytel solutions, organizing events, and exceeding quarterly targets through strategic, consultative selling and pipeline management.

Lead global IT strategy and operations for a life‑sciences CRO: oversee cloud and infrastructure, cybersecurity and compliance (GxP/21 CFR/GDPR), enterprise applications and data strategy, digital transformation, vendor and budget management, and build a global IT organization to enable clinical research, data science, and product delivery.