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CytelCY

Clinical Executive Consultant – Vice President

Cytel empowers life science leaders to maximize the potential of therapies through data and software solutions.

Cytel

Employee count: 1001-5000

United States only

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We are seeking a Vice President & Clinical Executive Consultant (CEC) to join our Streategic Consulting Team, whose mission is to deliver quantitative thought leadership across design, statistical methods, and decision-making during therapeutic product development. As a seasoned clinical development professional, you will expand Cytel’s reputation for innovation and thought leadership by guiding strategic engagements for pharmaceutical, biotech, and medical device clients. You will also build and maintain enduring client relationships in collaboration with Cytel’s business development teams and cross-functional colleagues.

In this senior advisory role, you will develop and demonstrate expertise in clinical trial design, statistical methodology, and strategic clinical development planning—ensuring Cytel remains at the forefront of industry innovation and enhancing our visibility and recognition across the global clinical development landscape.

We are seeking leaders with deep and broad experience designing and executing Phase I–IV clinical trials for novel therapeutics. Expertise in related quantitative domains—such as adaptive designs, clinical pharmacology, data science, or model-informed drug development—is highly advantageous. Depending on your skill set, the role may also include strategic consulting on clinical, safety/pharmacovigilance, regulatory, and market access pathways to accelerate patient access to new health technologies.

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About Cytel

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At Cytel, our mission is to unlock the power of data, empowering life science leaders to realise the full potential of therapies. We are committed to enhancing clinical decision-making through advanced software and data analysis tools. With a focus on innovation and excellence, Cytel partners with biopharmaceutical companies, providing them with solutions that leverage our deep understanding of statistics and trial design.

Our extensive expertise allows us to support clients at every stage of the clinical development process. From preclinical to post-market studies, we aim to optimize trial outcomes and ensure success in the competitive landscape of life sciences. By leveraging our comprehensive suite of services, we help clients navigate complex regulatory environments and make informed decisions based on robust data insights.

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