Associate Director, Statistical Programming

Associate Director, Statistical Programming

Full-Time 90000 - 126100 £ / year (est.) Home office (partial)
Healthcare Businesswomen’s Association

At a Glance

  • Tasks: Lead statistical programming for innovative drug development projects and empower high-performing teams.
  • Company: Join Novartis, a leader in transforming medicine with a commitment to diversity and inclusion.
  • Benefits: Competitive salary, performance bonuses, flexible working, and comprehensive wellbeing resources.
  • Other info: Dynamic, global environment with opportunities for professional growth and development.
  • Why this job: Shape the future of healthcare while making a real impact on patients' lives.
  • Qualifications: Degree in life sciences or related field, with proven leadership and statistical programming experience.

The predicted salary is between 90000 - 126100 £ per year.

Salary Range: £67,900.00 - £126,100.00

Location: London, UK. Remote working can be considered. This role is based in London, UK. Novartis is unable to offer relocation support for this role. Please only apply if this location is accessible for you.

Step into a high-impact leadership role where your expertise will shape the future of drug development. As Associate Director Statistical Programming, you will lead a high-performing community of programmers, driving innovation, quality, and efficiency across complex clinical programs. You’ll play a critical role in delivering timely, high-quality insights that enable life‑changing treatments to reach patients faster—while empowering teams, advancing technology adoption, and influencing global strategy across Novartis.

Key responsibilities:

  • Lead statistical programming activities as a Lead/Program Programmer for a large‑sized or complex project or group of projects globally or locally, or disease area with phase I to IV clinical studies in Novartis Global Drug Development.
  • Co-ordinate activities of programmers either internally or externally.
  • Make statistical programming decisions and propose strategies at project or disease level.
  • Develop statistical programming strategy and scientific documentation for the project(s) or disease area together with the Biostatistician(s).
  • Accountable for the assignment of resources and workload within his/her TA community and ensures sharing of resources between groups in order to meet company objectives and priorities.
  • May act as functional manager of local/global associates including providing supervision and advice to these programmers on functional expertise and processes.
  • Build and maintain effective working relationships with cross‑functional teams including Biostatistics and Data Management counterparts, able to summarize and discuss status of deliverables and critical programming aspects, such as, timelines, scope, and resource planning.
  • SP representative at project level and in the Submission team, or in local leadership team.
  • Develop programming strategy to drive standardization across studies or programs and effectively adopt R packages (e.g. Tidyverse), R Shiny Applications, AI‑enabled tools etc. to support data visualization, version control (e.g. Git‑based), and reproducible workflows.
  • Partner with the functional mentors to support capability development, appropriate tool adoption, and alignment with standards and business needs.
  • Accountable for timely and quality development and validation of all statistical programming components on assigned project(s).
  • Responsible for quality control and audit readiness of all assigned statistical programming deliverables as well as accuracy and reliability of statistical analysis results.
  • Provide authoritative technical and professional recommendations as representative of the statistical programming function at project level or for a major non‑clinical initiative.
  • Provide thought leadership level support and guidance.

Essential Requirements:

  • 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.

Benefits & Rewards:

At Novartis, we’re committed to reimagining medicine together - and rewarding the people who make it happen. Expected Annual Base Salary Range for role: £67,900.00 - £126,100.00. The base salary offered is determined based on gender‑neutral objectives, such as relevant skills, competencies and experience in accordance with the Novartis pay setting policy and upon joining Novartis will be reviewed periodically. In addition to your base salary, you may be eligible for a performance‑based bonus depending on certain performance parameters. The rewards of being part of our team go far beyond base pay and incentives. We also offer a variety of competitive benefits in kind to help you thrive personally and professionally, such as insurance plans, retirement plans, wellbeing resources and global recognition programs. In addition, we provide flexible and hybrid working options, where possible, and minimum 14 weeks paid parental leave. Pay equity is a fundamental principle of our employment policy and reflects our commitment to create a diverse, equitable and inclusive environment that treats all employees with dignity and respect, as outlined in our Code of Ethics. Note: Benefits and compensation may vary by country and are subject to local legal requirements, including provisions of collective bargaining agreements where applicable. A full overview of your compensation package, including any relevant collective bargaining agreement details applicable to your role based on your employment location and Novartis employer entity, will be communicated separately to you during the application process.

Commitment to Diversity and Inclusion: Novartis is committed to building an outstanding, inclusive work environment and diverse teams’ representative of the patients and communities we serve.

Skills Desired:

  • Classification Systems
  • Clinical Trials
  • Computer Data Storage
  • Computer Programming
  • Cross‑Functional Teams
  • Data Analysis
  • Data Structures
  • Initiative
  • People Management
  • Programming Languages
  • Reporting
  • Statistical Analysis
  • Waterfall Model

Associate Director, Statistical Programming employer: Healthcare Businesswomen’s Association

At Novartis, we pride ourselves on being an exceptional employer that fosters a culture of innovation and collaboration. As an Associate Director in Statistical Programming based in London, you will not only lead a talented team but also have access to competitive benefits, flexible working options, and robust opportunities for professional growth. Join us in our mission to reimagine medicine and make a meaningful impact on patients' lives while enjoying a supportive and inclusive work environment.

Healthcare Businesswomen’s Association

Contact Details:

Healthcare Businesswomen’s Association Recruitment Team

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We think you need these skills to ace Associate Director, Statistical Programming

Statistical Programming
Leadership Skills
Collaboration Skills
Organisational Skills
Clinical Trials Methodology
Good Clinical Practice (GCP)
Data Analysis

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