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Cytel

Senior Director, Innovative Statistics
United KingdomPermanentRemoteFull-TimeLead

Posted today

Description

Job Description
This role is ideal for a leader with a strong foundation in statistics and broad expertise in areas such as adaptive designs, innovative designs, clinical development strategy, data science, or model-informed drug development. You will provide strategic guidance to help clients define optimal regulatory, clinical, and market access pathways, ultimately supporting faster patient access to better health technologies.

Responsibilities
  • Provide strategic advice on client projects, working closely with Strategic Consultants and Analysts to define optimal regulatory, clinical, and/or market access strategies.
  • Develop innovative, tailored solutions by combining established methodologies with novel statistical and analytical approaches.
  • Lead assigned Strategic Consulting accounts and projects, serving as the primary client contact for consulting engagements.
  • Build trusted, long-term partnerships with clients and take ownership of their strategic needs.
  • Contribute to Cytel’s thought leadership in statistical methodology and clinical development strategy.
  • Identify, develop, and pursue new business opportunities within Strategic Consulting and across Cytel’s broader business units.
  • Recognize emerging client needs and design solutions that support revenue growth, profitability, and customer satisfaction.
  • Represent Cytel externally, raising brand awareness and strengthening the company’s position as an industry leader.
  • Travel regularly and engage directly with senior management and executive-level stakeholders at prospective and existing clients.
  • Build and leverage strong relationships across internal teams and external client organizations.

Qualifications
  • Advanced understanding of the biopharmaceutical R&D process, combined with strong business acumen and awareness of broader industry challenges.
  • Strong statistical expertise, with experience in areas such as adaptive designs, clinical development, data science, regulatory strategy, or model-informed drug development.
  • Strategic thinker with a global mindset, strong analytical skills, and the ability to solve complex problems.
  • Comfortable engaging with and presenting to senior executives and decision-makers.
  • Experience interacting with regulatory agencies such as the FDA and EMA, as well as key opinion leaders, to enhance clinical development plans.
  • Proven leadership and management skills, including the ability to build, mentor, and motivate teams of consultants and analysts.
  • Collaborative, entrepreneurial, and self-motivated, with the ability to thrive in a fast-paced, high-growth environment.
  • Master’s degree in Mathematics, Biostatistics, or a related field required; PhD preferred.
  • MBA, MD, or other advanced degree is highly desirable.
  • 10–15 years of experience in clinical trials, health research, or a related environment.

Why Join Cytel?
  • Play a meaningful role in helping clients and the wider industry shape the future of drug development.
  • Join Cytel during an exciting period of growth, with opportunities to progress into senior leadership roles.
  • Work alongside some of the brightest minds in biostatistics, clinical development, and data science.
  • Contribute to innovative approaches that help bring safe and effective health technologies to patients faster.

Cytel Inc. is an Equal Employment / Affirmative Action Employer. Applicants are considered for all positions without regard to race, color, religion, sex, national origin, age, veteran status, disability, sexual orientation, gender identity or expression, or any other characteristics protected by law.
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Cytel

Pioneers in data science advancing clinical research and accelerating therapies to patients

CambridgeContract Research1000+
Cytel logo

Cytel

Contract Research

Shape the future of drug development alongside 2,000 pioneering data scientists and biostatisticians. Tackle the industry's most complex clinical trials, drive regulatory innovation, and see your work accelerate life-changing treatments to patients.