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Global drug and device development services

Associate Statistical Programmer

Quantitative Biology & BiostatisticsConfirmed live in the last 24 hours
Full-timeBengaluru, Karnataka, IndiaNo salary listedIn-person

About the Job

Requirements

  • The candidate should have 0–2 years of relevant internship experience and hands-on experience in R programming, with basic SAS experience; clinical research industry experience is preferred.
  • The candidate must be able to perform assigned tasks under supervision, as appropriate to the role level.
  • The candidate must be able to liaise professionally with team members and work independently as well as within a team.
  • The candidate should have problem-solving and organizational skills, attention to detail, and verbal and written communication skills.
  • The candidate must demonstrate an ability to learn new applications and techniques.
  • The candidate should have basic knowledge of software products and platforms such as UNIX and Windows.
  • The candidate should have basic knowledge of statistical concepts, clinical research data structures, and the software development lifecycle.
  • The candidate should understand the development and use of standard programs and macros.
  • The candidate must have a master’s or bachelor’s degree in a quantitative or scientific discipline, or local equivalent.
  • The candidate must have the legal right to work in the country where the role is based.

Responsibilities

  • Create, validate, and execute statistical programs to generate analysis datasets, tables, figures, listings, and safety outputs, ensuring deliverables are accurate, complete, consistent, and completed according to established procedures and project timelines.
  • Adhere to assigned ICON and sponsor standard operating procedures and working procedures.
  • Record billable and non-billable time accurately in the appropriate time-management system.
  • Complete assigned mandatory ICON and sponsor training.
  • Follow programming specifications and study-specific requirements, including completing and filing required documentation.
  • Plan and organize workload to manage time effectively and meet project-specific timelines.
  • Use SAS and R efficiently and follow applicable programming guidelines.
  • Create high-quality, accurate safety and efficacy outputs, including analysis datasets, tables, figures, and listings.
  • Validate safety and efficacy outputs according to departmental procedures.
  • Create basic macros at the table, listing, and figure level.
  • Troubleshoot and resolve programming issues in a timely and efficient manner.
  • Travel domestically and/or internationally approximately 0% of the time.

Desired Qualifications

  • Experience in the clinical research industry is preferred.

About the Company

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Global drug and device development services

This company provides consulting, development, and commercialization support for drugs and medical devices through a global network of offices. Its team across 53 countries offers end-to-end services, from strategy and regulatory work to manufacturing and market access, helping clients shorten development time, lower costs, and raise quality. It differentiates itself with wide geographic reach and a clear focus on reducing time to market and cost while leveraging deep experience across many therapeutic areas. Its goal is to help clients accelerate the development of life-saving products and improve quality of life by delivering reliable information, practical solutions, and solid performance.

Company size
10,001+
Company stage
IPO
Headquarters
Ireland
Founded
1990

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