Jobs at Cytel

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 Clinical Data Manager II ensures accuracy and consistency of clinical trial data while managing access in data management systems and collaborating with cross-functional teams.

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.

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

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

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

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 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.

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