Statistical Programmer

Roles and responsibilities

Clements Partners is proud to partner with leading pharmaceutical organizations in connecting exceptional talent with meaningful career opportunities. We are currently seeking a skilled Statistical Programmer to join the team of our client, a major player in the pharmaceutical industry. This is a fully remote position, available to candidates across the EMEA (Europe, the Middle East, and Africa) region. This role offers an exciting opportunity to contribute to cutting-edge clinical studies while working from the comfort of your home.

Role Overview:

As a Statistical Programmer, you will play a critical role in the development and execution of SAS programs for clinical data analysis, ensuring all outputs adhere to industry regulations and standards, including CDISC, SDTM, and ADaM. You will work closely with cross-functional teams, including statisticians, data managers, and clinical researchers, to prepare statistical analysis plans (SAPs) and deliver high-quality data outputs.

Key Responsibilities:

• SAS Programming for Clinical Data: Design, develop, and implement SAS programs to support the analysis of clinical trial data. This will involve the preparation of tables, listings, and figures (TLFs), as well as ensuring the accurate transformation and reporting of clinical data.

• Adherence to Regulatory Standards: Ensure that all programming and data outputs comply with regulatory standards, including CDISC standards (SDTM, ADaM) and applicable industry guidelines. You will maintain a keen understanding of evolving regulatory requirements and industry best practices.

• Collaboration and Communication: Work closely with statisticians and other clinical trial team members to prepare and refine Statistical Analysis Plans (SAPs). Effective communication is key to ensuring that programming efforts align with project goals, timelines, and quality expectations.

• Data Validation and Quality Control: Support the validation and quality assurance of datasets and programming outputs to ensure accuracy and integrity in clinical study results. Troubleshoot any discrepancies or issues that arise during data processing, and implement improvements to programming processes for increased efficiency.

• Continuous Learning and Improvement: Stay up-to-date on the latest industry trends, regulatory changes, and programming techniques. Engage in ongoing professional development to continually improve your programming skills and contribute to process improvements.

Desired candidate profile

Qualifications:

• A Bachelor’s degree in Statistics, Computer Science, or a related field.
• Demonstrated expertise in SAS programming (BASE, MACRO, STAT) with hands-on experience in clinical trials within the pharma, biotech, or CRO environment.
• Strong understanding of CDISC standards (SDTM, ADaM) and experience applying them to clinical data.
• Detail-oriented, with excellent organizational and communication skills, and a strong ability to collaborate with cross-functional teams.

This position provides an excellent opportunity to work with a forward-thinking pharmaceutical company on impactful clinical studies while enjoying the flexibility of remote work. If you are an experienced SAS programmer looking to advance your career and make a difference in the pharmaceutical field, we would love to hear from you.

Join our client's team and be a part of shaping the future of healthcare!