Clinical SAS Programmer Job Description [Updated for 2025]

In the healthcare sector, the demand for Clinical SAS Programmers is increasingly prominent.

As medical technology continues to advance, the need for proficient individuals who can design, develop, and maintain our clinical data systems becomes more urgent.

But let’s delve deeper: What’s truly expected from a Clinical SAS Programmer?

Whether you are:

• A job seeker trying to understand the core of this role,
• A hiring manager outlining the ideal candidate,
• Or simply intrigued by the intricacies of Clinical SAS Programming,

You’re in the right place.

Today, we introduce a customizable Clinical SAS Programmer job description template, designed for easy posting on job boards or career sites.

Let’s dive right in.

Clinical SAS Programmer Duties and Responsibilities

Clinical SAS Programmers are responsible for developing, implementing and maintaining software systems used in clinical trials and research.

They use SAS software to manipulate and manage clinical data, generate analysis datasets, tables, listings, and figures and to ensure that results meet the standards and requirements set by the respective industry.

The main duties and responsibilities of a Clinical SAS Programmer include:

• Developing, testing, validating, and maintaining SAS programs to generate analysis datasets, tables, listings, and figures
• Working closely with data management and statistical teams to understand the requirements for each project
• Reviewing clinical trial data and addressing any data inconsistencies or errors
• Designing and implementing strategies to manage, clean and verify clinical trial data
• Performing statistical analysis on clinical trial data
• Creating and maintaining documentation for all SAS programs and processes
• Ensuring that all programming activities and processes performed are conducted according to standard operating procedures and good programming practices
• Contributing to the development of standard operating procedures, guidelines, and best practices for SAS programming

 

Clinical SAS Programmer Job Description Template

Job Brief

We are looking for a highly skilled Clinical SAS Programmer to join our team.

The successful candidate will be responsible for developing, maintaining, validating, and running clinical trial reporting systems using SAS.

Duties also include generating statistical summaries, listings and graphs for reports, and performing quality control checks on SAS programs to ensure the accurate and reliable performance of their functions.

 

Responsibilities

• Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs.
• Validate SAS programs and other statistical analyses developed by other programmers.
• Create and maintain documentation for all programming activities.
• Assist with the development of statistical analysis plans.
• Provide input into clinical trial protocols and case report forms.
• Perform ad hoc statistical analyses as requested.
• Ensure data consistency and integrity.
• Meet project timelines and deliverables.

 

Qualifications

• Proven work experience as a Clinical SAS Programmer.
• Experience in developing and validating SAS programs in a clinical research environment.
• Excellent knowledge of CDISC SDTM and ADaM data models.
• Strong statistical analysis skills.
• Attention to detail and problem-solving skills.
• Proficient in the use of SAS Macro language and other advanced SAS features.
• Excellent written and verbal communication skills.
• BSc or higher degree in Statistics, Mathematics, Computer Science or a related field.

 

Benefits

• 401(k)
• Health insurance
• Dental insurance
• Retirement plan
• Paid time off
• Professional development opportunities

 

Additional Information

• Job Title: Clinical SAS Programmer
• Work Environment: Office setting with the option for remote work. Some travel may be required for meetings or to visit clinical sites.
• Reporting Structure: Reports to the Clinical Data Manager or Director of Biostatistics.
• Salary: Salary is based upon candidate experience and qualifications, as well as market and business considerations.
• Pay Range: $85,000 minimum to $125,000 maximum
• Location: [City, State] (specify the location or indicate if remote)
• Employment Type: Full-time
• Equal Opportunity Statement: We are an equal opportunity employer and value diversity at our company. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.
• Application Instructions: Please submit your resume and a cover letter outlining your qualifications and experience to [email address or application portal].

 

What Does a Clinical SAS Programmer Do?

Clinical SAS Programmers work within the biotechnology, pharmaceutical, and healthcare industries.

They are typically engaged by these organizations to manage, organize, and analyze clinical trial data.

They use Statistical Analysis System (SAS) software to develop, code, and debug programs that analyze and interpret clinical trial data.

This data is then used to support the results of clinical trials and the development of new treatments or medications.

Clinical SAS Programmers often work closely with data managers and biostatisticians to understand the data and design the appropriate analysis programs.

They also create tables, listings, and figures to visualize the data and present it in a way that is understandable to non-technical stakeholders.

In addition, they validate and document the programs to ensure they meet regulatory and company standards.

If any issues or inconsistencies arise in the data, the Clinical SAS Programmer is responsible for resolving these and ensuring the integrity of the data.

Their work is crucial in the drug development process, as the results they produce from the clinical trial data can directly impact decisions about the safety and efficacy of the treatments being tested.

 

Clinical SAS Programmer Qualifications and Skills

Clinical SAS Programmers utilize technical skills, analytical thinking, and a deep understanding of clinical trials to develop, modify, maintain, and validate SAS programs for statistical analysis.

The necessary skills and qualifications for a Clinical SAS Programmer include:

• Proficiency in SAS programming language to write, debug, and validate code for statistical analysis and reporting in clinical trials.
• Analytical skills to understand and interpret statistical analysis plans, and implement them in SAS programs.
• Communication skills to effectively collaborate with Statisticians, Data Managers, and Clinical Study Managers, and to present analysis results in a clear and comprehensible way.
• Attention to detail to ensure data accuracy, and to identify and resolve any issues in the SAS programs.
• Understanding of clinical trial data and processes, as well as knowledge of FDA guidelines and regulations for clinical data reporting.
• Problem-solving skills to troubleshoot and resolve programming issues, and to adapt to changes in study design or analysis requirements.
• Time management skills to manage multiple projects simultaneously and meet deadlines.

 

Clinical SAS Programmer Experience Requirements

Entry-level Clinical SAS Programmers typically have a Bachelor’s degree in Biostatistics, Computer Science, or a related field with 1 to 2 years of experience gained through internships or part-time roles in clinical research or pharmaceutical industries.

These professionals also gain practical experience in SAS programming, data management, and analysis during their academic training.

Candidates with 2 to 3 years of experience often refine their SAS programming skills and gain expertise in clinical trial data analysis and reporting.

Experience in using SAS to produce tables, listings, and graphs (TLGs) for clinical trial reports is often required.

They may also gain experience in other related roles such as Data Analyst or Clinical Data Manager.

Professionals with more than 3 years of experience likely have proficiency in handling large datasets, knowledge of regulatory requirements, and experience in working on different phases of clinical trials.

They might also have some experience in protocol development, statistical analysis plan (SAP) development, and coordinating with other clinical team members.

Those with over 5 years of experience often possess advanced SAS programming skills and have substantial experience in managing clinical trial data and producing statistical reports.

They may have also gained some leadership experience, and thus could be suitable for senior roles such as Lead SAS Programmer or Biostatistics Manager.

Such roles often require experience in mentoring junior programmers, managing projects, and liaising with stakeholders.

 

Clinical SAS Programmer Education and Training Requirements

Clinical SAS Programmers generally hold a bachelor’s degree in biostatistics, computer science, data science, or a related field.

A strong background in programming, especially in the SAS language, is crucial for this role.

They are also expected to have knowledge of databases, SQL, and other relevant software.

Experience with clinical trials and FDA regulations is often required, as the role involves programming for clinical research.

Knowledge in the medical or pharmaceutical field can be beneficial.

Some roles may require a master’s degree or higher, especially in biostatistics or a related field, for more complex responsibilities or leadership positions.

Certifications, such as the SAS Certified Clinical Trials Programmer, can showcase a candidate’s proficiency in SAS programming and understanding of clinical trials data.

Continued education and training are important in this role due to the dynamic nature of clinical research and evolving programming languages and techniques.

 

Clinical SAS Programmer Salary Expectations

The average salary for a Clinical SAS Programmer is $87,667 (USD) per year.

However, the exact salary can vary depending on factors such as experience, education, the complexity of the projects handled, and the location of the job.

 

Clinical SAS Programmer Job Description FAQs

What skills does a Clinical SAS Programmer need?

A Clinical SAS Programmer should possess a strong background in statistics and data analysis, along with proficiency in SAS programming.

They should also have a deep understanding of clinical trial processes and regulatory requirements.

Good communication skills are crucial as they have to collaborate with biostatisticians, data managers, and other team members.

Attention to detail is important to ensure the accuracy of data analysis and reports.

 

Does a Clinical SAS Programmer require a specific degree?

Clinical SAS Programmers typically have a degree in Statistics, Mathematics, Computer Science, or a related field.

Additionally, a postgraduate degree or experience in Clinical Research or Biostatistics can be beneficial.

There are also SAS certification programs that can validate their programming skills and improve job prospects.

 

What should I look for in a Clinical SAS Programmer’s resume?

Apart from educational qualifications, look for their proficiency in SAS, SQL, and other programming languages.

Experience in clinical research, data management, and biostatistics is highly desirable.

Any certifications such as Base SAS Programmer Certification or Advanced SAS Programmer Certification are definite pluses.

Also, check for their understanding of CDISC standards and FDA regulations.

 

What qualities make a good Clinical SAS Programmer?

A good Clinical SAS Programmer is a problem-solver who can handle complex data and translate it into meaningful insights.

They should be detail-oriented to ensure accuracy in their work.

Good communication skills are needed to liaise with different team members and stakeholders.

They should also be able to work under pressure and meet deadlines as clinical trials are often time-sensitive.

 

Is it challenging to hire a Clinical SAS Programmer?

Hiring a Clinical SAS Programmer can be challenging due to the specific skill set required for the role.

The candidate should not only be proficient in SAS programming, but also have an understanding of clinical trials, statistical analysis, and regulatory guidelines.

The demand for SAS programmers in the clinical research field is high, hence there can be a lot of competition for qualified candidates.

 

Conclusion

And there you have it.

Today, we’ve demystified the vital role of a Clinical SAS Programmer in the healthcare sector.

Surprised?

It’s not just about managing databases.

It’s about shaping the future of healthcare, one data analysis at a time.

With our comprehensive Clinical SAS Programmer job description template and real-world scenarios, you’re prepared to take the next leap.

But why halt your journey here?

Dig deeper with our job description generator. It’s your ultimate tool for creating precise job postings or refining your resume to absolute perfection.

Remember:

Every data analysis is a piece of the larger healthcare puzzle.

Let’s shape that future. Together.

How to Become a Clinical SAS Programmer (Complete Guide)

Flexible and Forward: Jobs That Move with Your Life

The Offbeat Job Market: Exploring the Weirdest Careers

Relaxing Routines: Jobs Where Monday Blues Are Nonexistent

Workday Glee: Enjoyable Careers That Keep You Grinning