Junior Statistical Programmer Analyst -Permanent Role

clinchoice; United States; On-site; USD 60,000 - 90,000; Full time

Job summary

ClinChoice is seeking a Junior Statistical Programmer to join our in-house team supporting clinical trials across a diverse client portfolio in pharma, biotech, medical devices and consumer health. Under supervision, you will develop, validate and maintain SAS and/or R deliverables, and contribute to SDTM/ADaM datasets and CDISC standards.

You will work with Senior Programmers, Biostatisticians, and Data Managers to ensure quality, timeliness, and regulatory-ready outputs while expanding

Qualifications

• 0-2 years of experience in statistical programming within pharma/biotech/CRO
• Basic to intermediate knowledge of SAS and/or R
• Familiarity with SAS programming and SAS Macro language is preferred
• Basic understanding of clinical trial data and drug development process
• Knowledge or exposure to CDISC SDTM/ADaM is preferred
• Familiarity with clinical trial datasets, tables, figures, and listings is an advantage
• Strong attention to detail and commitment to data quality
• Ability to work in a team and learn from seniors
• Ability to manage tasks and meet timelines

Responsibilities

• Support development and validation of datasets, tables, figures, and listings for clinical trials.
• Perform programming activities using SAS and/or R under guidance.
• Assist with data processing and integration from internal and external sources.
• Support ad hoc analyses and programming activities for clinical development.
• Assist with development, review, and maintenance of programming specifications and documentation.
• Contribute to SDTM and ADaM datasets and specifications.
• Support preparation and review of Define-XML and other regulatory documents.
• Collaborate with Senior Programmers, Biostatisticians, Data Managers and cross-functional teams.

Skills

SAS programming

R programming

SAS Macro language

Statistical programming basics

Teamwork

Education

Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Engineering, Life Sciences, or related discipline

Tools

SAS

R

CDISC (SDTM/ADaM)

Job description

ClinChoice is a global full-service CRO committed to professional growth and a quality-driven "one-team" culture. We are seeking a Junior Statistical Programmer to join our in-house team and support projects across a diverse client portfolio, including pharmaceutical, biotechnology, medical device, and consumer health companies of varying sizes.

The Junior Statistical Programmer is a delivery-focused role supporting clinical trial programming activities under the guidance and supervision of experienced Statistical Programmers and Programming Team Leaders. The individual will contribute to the development, validation, and maintenance of statistical programming deliverables and gain hands-on experience in clinical trial data and industry standards.

The role requires a strong foundation in statistical programming, attention to detail, willingness to learn, and the ability to work effectively within a collaborative team environment.

Responsibilities

Programming for Clinical Trials

• Support the development and validation of datasets, tables, figures, and listings for clinical trials.
• Perform programming activities using SAS and/or R under appropriate guidance and review.
• Assist with processing and integrating data from internal and external sources.
• Support ad hoc analyses and programming activities for clinical development and other Research & Development functions.
• Assist with the development, review, and maintenance of programming specifications and documentation.
• Contribute to the development and review of SDTM and ADaM datasets and specifications .
• Support the preparation and review of Define-XML and other clinical trial documentation.
• Work closely with Senior Statistical Programmers, Biostatisticians, Data Managers, and other cross-functional team members.

Electronic Submissions

• Support the programming and validation of CDISC-compliant datasets and deliverables for regulatory submissions.
• Assist with the preparation of supporting documentation for electronic submissions.
• Ensure programming outputs follow applicable standards, specifications, and quality requirements.

Quality and Validation

• Perform programming validation and quality checks according to established procedures.
• Identify, document, and resolve programming issues in collaboration with senior team members.
• Ensure assigned deliverables are completed accurately and within agreed timelines.

Standards and Guidelines

• Follow departmental programming standards, working instructions, and applicable industry guidelines.
• Develop knowledge of CDISC standards, including SDTM and ADaM .
• Assist in maintaining and improving programming macros, utilities, and reusable functions.

Qualification & Experience

• Bachelor's or Master's degree in Computer Science, Statistics, Mathematics, Engineering, Life Sciences, or a related discipline .
• 0-2 years of experience in statistical programming, preferably within the pharmaceutical, biotechnology, CRO, or clinical research industry.
• Basic to intermediate knowledge of SAS and/or R .
• Familiarity with SAS programming and SAS Macro language is preferred.
• Basic understanding of clinical trial data and the drug development process .
• Knowledge or exposure to CDISC standards, SDTM, and ADaM is preferred.
• Familiarity with clinical trial datasets, tables, figures, and listings is an advantage.
• Strong attention to detail and commitment to data quality.
• Ability to work effectively in a team environment and learn from senior team members.
• Ability to manage assigned tasks and meet project timelines.

About ClinChoice

ClinChoice is a global full-service CRO specializing in clinical development and functional solutions for pharmaceutical, biotechnology, medical device, and consumer health companies. We have over 28 years of proven high-quality delivery and results across all our services, with over 4,000 professionals in more than 20 countries across the Americas, Europe, and Asia-Pacific.

Our Company Ethos

Our mission drives our culture: to contribute to a healthier and safer world by accelerating the development and commercialization of innovative drugs and devices. Our employees are the most valuable company asset and they are the fulcrum around which all ClinChoice activities are built and close management and training is the core instrument to develop and maintain highly-qualified personnel. The continuous training keeps the resources qualified in terms of competence and expertise and gives all personnel the clear tools needed to manage both internal and client processes with the same methodology. The success of these core values is