Associate Statistical Programmer
- Compensation
- Not disclosed
- Location
- India, Bangalore
- Work setup
- Not specified
- Seniority
- Intern
- Employment
- Internship
- Experience
- 0+ years
- Category
- Not specified
- Posted
Skills
Must have
- 0-2 years of prior relevant Internship and hand’s on in R programming with basic experience in SAS, preferably in the clinical research industry.
- Ability to perform assigned tasks under supervision, as appropriate to the level.
- Ability to liaise professionally with team members.
- Ability to work independently and as part of a team environment.
- Good problem-solving and organizational skills, attention to detail, and verbal and written communication skills.
- Demonstrated ability to learn new applications and techniques.
- Basic knowledge of relevant software products and platforms, such as UNIX and Windows.
- Basic knowledge of statistical concepts.
- Basic knowledge of data structures used in the clinical research industry and the software development lifecycle.
- Understanding of the development and use of standard programs and macros.
- Master’s/bachelor’s degree, in quantitative or scientific discipline, or local equivalent.
Full description
Associate Statistical Programmer, BengaluruAt 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.
The Associate Statistical Programmer is responsible for creating, validating, and executing statistical programs to generate analysis datasets, tables, figures, listings, and safety outputs, ensuring all deliverables are accurate, complete, consistent, and completed in line with established procedures and project timelines.
What You Will Do:
- Recognize, exemplify and adhere to ICON's values, centred around our commitment to People, Clients and Performance.
- Embrace and contribute to a culture of process improvement, with a focus on streamlining processes, adding business value and meeting client needs.
- Travel, approximately 0%, domestically and/or internationally.
- Read, understand and adhere to all assigned ICON and sponsor standard operating procedures and working procedures.
- Record all billable and non-billable time accurately in the appropriate time-management system.
- Complete all assigned mandatory ICON and sponsor training.
- Adhere to programming specifications and study-specific requirements, including completion and filing of required documentation.
- Plan and organize workload to ensure effective time management and adherence to project-specific timelines.
- Use SAS/R efficiently and follow applicable SAS/R programming guidelines.
- Create safety and efficacy outputs, including analysis datasets, tables, figures and listings, to a high standard of quality and accuracy.
- Validate safety and efficacy outputs in accordance with departmental procedures.
- Create basic macros at the table, listing and figure level.
- Troubleshoot and resolve programming issues in a timely and efficient manner.
Your Profile:
- 0-2 years of prior relevant Internship and hand’s on in R programming with basic experience in SAS, preferably in the clinical research industry.
- Ability to perform assigned tasks under supervision, as appropriate to the level.
- Ability to liaise professionally with team members.
- Ability to work independently and as part of a team environment.
- Good problem-solving and organizational skills, attention to detail, and verbal and written communication skills.
- Demonstrated ability to learn new applications and techniques.
- Basic knowledge of relevant software products and platforms, such as UNIX and Windows.