Statistical Programmer

Roles and responsibilities

At Clements Partners, we specialize in connecting top talent with leading pharmaceutical organizations. We are currently working with a renowned pharmaceutical client who is looking to add a highly skilled Statistical Programmer to their team. This is a fully remote opportunity available for candidates across the EMEA (Europe, Middle East, and Africa) region, allowing you to contribute to impactful clinical studies from the comfort of your own home.

Key Responsibilities:

As a Statistical Programmer, your primary role will be to design and develop high-quality SAS programs to analyze clinical trial data in line with industry standards and regulatory guidelines. You will play a vital part in the end-to-end data management process, collaborating closely with cross-functional teams to ensure the accurate and efficient analysis of clinical data.

Specific duties will include:

• Designing and developing SAS programs for clinical data analysis, ensuring they meet regulatory standards such as CDISC (Clinical Data Interchange Standards Consortium), SDTM (Study Data Tabulation Model), and ADaM (Analysis Data Model).
• Collaborating with cross-functional teams (including biostatisticians, clinical researchers, and data managers) to prepare statistical analysis plans (SAPs) and ensure high-quality, consistent data outputs.
• Generating tables, listings, and figures (TLFs) based on clinical data, and supporting dataset validation to ensure the accuracy and integrity of clinical trial information.
• Troubleshooting and optimizing existing programming processes to enhance efficiency and ensure timely delivery of clinical study results.
• Maintaining up-to-date knowledge of the latest industry standards, regulatory changes, and best practices, ensuring that your programming techniques comply with both internal and external requirements.

Desired candidate profile

Qualifications:

The ideal candidate will have the following qualifications:

• A Bachelor’s degree in Statistics, Computer Science, or a related field.
• Proficiency in SAS programming (including BASE, MACRO, and STAT), with solid experience in SAS programming for clinical trials.
• Familiarity with CDISC standards (SDTM, ADaM) and experience implementing these standards in clinical research.
• Prior experience in SAS programming within the pharmaceutical, biotech, or CRO (Contract Research Organization) environment.
• Strong attention to detail, along with excellent organizational and communication skills to effectively collaborate with teams and stakeholders.

This remote role offers an exciting opportunity to contribute to meaningful clinical studies, using your programming expertise to make a difference in the development of pharmaceutical treatments. If you're looking for a dynamic and flexible role within the pharma industry, this could be the perfect fit for you.