Statistical Programmer 2

IQVIA; Bellville; On-site; ZAR 600,000 - 900,000; Full time

Job summary

IQVIA is seeking a skilled Statistical Programmer to develop, maintain, and support programs for client needs. You will plan and lead project-related statistical programming activities and serve as a technical resource within the Statistical Programming department.

Responsibilities include programming tables, figures, listings; validating databases; integrating data from multiple studies; documenting programming processes; mentoring junior staff; and managing scope, effort, and timelines under

Qualifications

• Master's or Bachelor's degree with relevant experience.
• Knowledge of statistics and clinical drug development processes.
• Experience with SAS programming in a research or submission setting.
• Strong organizational and communication skills.

Responsibilities

• Plan, perform, test, and document programs for tables, figures, and listings.
• Program databases and manage data transfers for clients.
• Plan database validation and quality control activities.
• Integrate databases from multiple studies or sources.
• Develop and maintain programming documentation.
• Provide advanced technical expertise to stakeholders and deliver solutions.
• Mentor junior staff and guide onboarding.
• Estimate effort and manage scope and budgets for studies.

Skills

Leadership

Communication

Project management

Mentorship

Organizational skills

Attention to detail

Education

Master's degree in Computer Science or related field

Bachelor's degree in Computer Science or related field

Equivalent education/experience

Tools

Base SAS

SAS/STAT

SAS Macro Language

Job description

Job Overview

Provide advanced technical expertise to develop, maintain, and support programs that meet internal and external client needs. Plan and lead the development of project-related solutions covering the full scope of statistical programming activities. Serve as a technical resource within the Statistical Programming department.

Essential Functions

• Plan, perform, test, and document programs used to produce statistical tables, figures, and listings.
• Program analysis databases (derived datasets) and manage data transfers for internal and external clients.
• Plan and perform database quality control and validation activities, as required.
• Program the integration of databases from multiple studies or data sources.
• Develop and maintain programming documentation, including plans and specifications, as appropriate.
• Provide advanced technical expertise to internal and external stakeholders and independently deliver project solutions to teams and the department.
• Plan, develop, implement, and validate new processes, technologies, macros, and applications.
• Fulfill project responsibilities at the level of statistical team lead for single studies, under supervision.
• Understand project Scope of Work, estimate completed effort, and manage out-of-scope activities for single studies.
• May manage budgets and resource requirements, and provide revenue and resource forecasts for single studies.
• May be required to understand and apply budgeting and quoting assumptions.
• Provide training, mentorship, and guidance to junior and newly onboarded staff.

Qualifications

• Master’s degree in Computer Science or a related field with a minimum of one year of relevant experience, or
• Bachelor’s degree in Computer Science or a related field with a minimum of two years of relevant experience, or
• An equivalent combination of education, training, and experience.
• Knowledge of statistics, programming, and/or the clinical drug development process.
• Working knowledge of computing applications, including Base SAS, SAS/STAT, and SAS Macro Language.
• Strong organizational, interpersonal, leadership, and communication skills.
• Ability to manage multiple tasks and projects effectively.
• Excellent attention to detail and accuracy.
• Ability to establish and maintain effective working relationships with coworkers, managers, and clients.