Associate Director, Statistical Programming
$84,875–$157,625 year
Hybrid · London, England, United Kingdom
Job Summary
Step into a high-impact leadership role steering statistical programming for large, complex clinical programs. Lead activities for global or local projects (Phase I–IV), coordinate internal and external programmers, set programming strategy and scientific documentation with Biostatisticians, manage resource allocation within the TA community, supervise local/global associates, and drive standardization across studies with modern tools (R, Shiny, Git) to deliver timely, high-quality insights. Partner with cross-functional teams to ensure timely and audit-ready deliverables, provide thought leadership, and influence global strategy in drug development.
Required Qualifications
- University or college degree in life science, computer science, data science, pharmacy, statistics, nursing or equivalent relevant degree
- Proven leadership, collaboration and organizational skills with demonstrated ability to successfully manage simultaneous trials and meet deadlines
- Excellent understanding of clinical trials methodology, GCP and medical terminology
- Must be able to anticipate challenges and risks and proactively suggest/implement solutions
- Ability to work under pressure demonstrating agility through effective and innovative team leadership
- Excellent interpersonal skills and proven ability to operate effectively in a global environment
- Foster a team environment that values learning, adaptability, and continuous improvement
- Ability to influence and communicate across functions and to external stakeholders
- Experience in Drug Development with experience in Statistical Programming Management or leadership experience
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