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Principal Statistical Programmer

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China, HangzhouPosted 9 h agoDirect from company

  • LocationChina, Hangzhou; Taiwan, Taipei; China, Shanghai
  • Work typeNot stated
  • EmploymentFull-time
  • Posted5 November 2026
  • SourceIcon's careers page (Workday)
  • Last checked2 h ago on Icon's careers page
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About the role

Principal Statistical Programmer At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise.

As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit patients worldwide.

As a Principal Statistical Programmer at ICON, you will be responsible for leading the design and implementation of statistical programming solutions that support clinical trials and regulatory submissions.

What You Will Do:
You will manage day-to-day statistical programming activities, supporting your team to deliver quality outcomes.

Key responsibilities include:

- Leading the development and validation of statistical programs for data analysis and reporting, ensuring compliance with regulatory standards.

- Collaborating with biostatisticians and clinical teams to define project requirements and ensure alignment with study objectives.

- Overseeing the creation of programming specifications, documentation, and technical reports for regulatory submissions.

- Providing mentorship and guidance to junior statistical programmers, fostering a culture of learning and continuous improvement.

- Staying current with industry trends and advancements in statistical programming to drive innovation and enhance project outcomes.

Your Profile:
You will have solid statistical programming experience, with the ability to manage competing priorities and develop your team.

Required qualifications and experience:

- Bachelor's degree in statistics, computer science, mathematics, or a related discipline

- Significant experience in statistical programming, particularly in the context of clinical trials and regulatory submissions.

- Expertise in programming languages such as SAS, R, or Python, with proficiency in data management and statistical analysis.

- Excellent problem-solving skills and attention to detail, with a commitment to delivering high-quality results.

- Strong communication and interpersonal skills, facilitating effective collaboration across teams and with stakeholders.

- A commitment to maintaining high standards of quality and compliance in all programming activities.

Employment with ICON is contingent upon having the legal right to work in the country where the role is based.

Rewards & Benefits
ICON offers a competitive and comprehensive total rewards package designed to support your health, wellbeing, and career development.

Benefits may include:

- Competitive base salary and performance related incentives

- Health and wellbeing programmes including medical, dental, and vision coverage where applicable

- Retirement and pension plans

- Life assurance and disability coverage

- Employee assistance programmes and wellbeing resources

- Learning and development opportunities through structured training and career pathways

Benefits may vary depending on role and location.

Visit our careers site to read more about the benefits ICON offers.

Inclusion and Accessibility
ICON is an equal opportunity employer. We are committed to building an inclusive and accessible workplace where everyone feels valued and supported.

If you require reasonable accommodations during the recruitment process, please let us know or submit a request  here .

Are you a current ICON Employee? Please click here to apply

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