Jobs at Cytel

Develop automation and AI solutions supporting pharmaceutical clinical trials. Interpret requirements, identify workflow improvements, build proof-of-concept tools using R, Shiny, and LLM-supported coding, and mature successful prototypes into validated, documented, reusable solutions. Collaborate with statisticians, programmers, data scientists, and AI leads while ensuring testing, traceability, audit trails, version control, and compliance with regulated clinical development expectations.

Lead statistical activities for Phase II–III clinical trials from protocol design through reporting. Responsibilities include SAP development, sample size calculations, statistical analysis, TLF review, database lock and submission support, regulatory responses, vendor oversight, and cross-functional collaboration. Use SAS and/or R for analyses, modeling, simulation, exploratory work, and quality control. Coordinate statistical activities across studies and apply adaptive, group sequential, count-data, machine learning, and deep learning methods.

Provides executive scientific and strategic leadership in quantitative clinical pharmacology consulting. Leads Pop-PK, PK-PD, NCA, MIDD, regulatory strategy, trial design, and quantitative decision-making engagements. Develops thought leadership, manages major client relationships, supports business development, mentors quantitative teams, and collaborates with statisticians, software teams, business developers, and data scientists. The role also involves regulatory authority engagement, technical oversight, publications, presentations, and client travel.

Leads moderately complex clinical trial projects, managing teams, client relationships, timelines, scope, budgets, quality, documentation, financial performance, and contractual requirements. Serves as the primary customer contact and communicates project status, forecasts, risks, and changes to sponsors and company management.

Drive revenue growth across the DACH territory by acquiring and managing customers, leading end-to-end consultative sales cycles, developing target accounts, managing pipelines, exceeding sales targets, and positioning Cytel’s services and solutions. The role includes territory strategy, executive-level client engagement, relationship building, industry events, and collaboration with internal experts and leadership.

The Principal Biostatistician leads clinical studies, provides statistical expertise for trial processes, and collaborates with sponsor teams on HTA submissions.

Lead statistical strategy and delivery for Phase I-IV clinical trials embedded with a pharmaceutical sponsor. Design analyses, support protocol and reporting activities, oversee programming/CRO work, apply SAS/R (R Shiny)/Python and ML/DL methods for analyses and automation, and mentor junior statisticians.

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 and perform SAS-based data manipulation, analysis, and reporting for Phase I–IV clinical trials; generate and validate SDTM/ADaM datasets and TLFs, perform QC/validation, produce submission documents (define.xml), create ad-hoc reports, support efficacy analyses, communicate with cross-functional teams, and provide study lead duties as needed.