Jobs at Cytel

The Executive Consultant will lead strategic consulting in Quantitative Clinical Pharmacology, mentor teams, and engage with clients for business development and scientific expertise.

The role involves developing and closing software business in clinical research organizations, executing sales strategies, and maintaining client relationships in the biopharmaceutical space.

The Senior Vice President of AI and Transformation will develop and deliver strategies for integrating AI, analytics, and automation into processes, ensuring they meet regulatory standards. This role involves partnership with leadership to enhance service quality and governance principles for responsible tech use.

The FP&A Analyst develops financial models and dashboards, supports forecasting and financial analysis, and partners with various teams to improve data integrity and financial processes.

The Principal Statistical Programmer will oversee and deliver statistical programming for clinical trials, ensure high-quality data summaries, and support regulatory submissions while collaborating with CROs and other functions.

As a Principal Biostatistician, you will lead Phase I-IV clinical trials, provide statistical support, oversee internal programming, and contribute to various statistical activities.

The Principal RWE Scientist leads studies using large healthcare data for evaluating clinical and economic outcomes, focusing on oncology and project execution management.

The role involves programming for clinical trial data management, ensuring data accuracy, collaborating with teams, and mentoring junior staff.

The Head of Quality Assurance will lead Cytel's global QA strategy, enhance the Quality Management System, and drive modernization through digital tools and automation. Responsibilities include managing audits, compliance, and mentoring a high-performing QA team.

The Senior Director, Portfolio Leadership is responsible for revenue growth, solution architecture, and client engagement, ensuring high-value offerings are aligned with client needs and market trends.

The role involves providing strategic statistical advice, developing innovative solutions for clients in the biopharmaceutical sector, and leading consulting projects to enhance brand recognition and client relationships.

The Principal Statistical Programmer supports Epidemiology by preparing Real World data, conducting analyses, programming data tools, and liaising with stakeholders on multiple projects. Responsibilities include creating analytical databases, producing reports, and managing relationships with clients and investigators.

The Senior Clinical Programmer will develop and maintain programming for clinical trial data, ensuring data quality and compliance, while collaborating with other stakeholders. Responsibilities include troubleshooting, documentation, and mentoring junior programmers.

The Senior Clinical Data Manager oversees comprehensive data management activities throughout the clinical trial process, ensuring compliance and quality of data. The role includes collaboration with stakeholders, handling regulatory submissions, and managing multiple drug development programs.

As a Principal Statistical Programmer, you'll generate datasets, oversee CRO deliverables, support clinical reports, and ensure compliance with FDA regulations.