Job Summary (Primary function) This role is responsible for processing clinical data required for ... Proficiency in using SAS to perform efficacy analyses and validate important data derivations when ...
Job Summary (Primary function) This role is responsible for processing clinical data required for ... Proficiency in using SAS to perform efficacy analyses and validate important data derivations when ...
Job Summary (Primary function) This role is responsible for processing clinical data required for ... Proficiency in using SAS to perform efficacy analyses and validate important data derivations when ...
Job Summary (Primary function) This role is responsible for processing clinical data required for ... Proficiency in using SAS to perform efficacy analyses and validate important data derivations when ...
Entry Level Clinical Sas Programmer information
See Delaware salary details
$19.25 - $24.80
4% of jobs
$24.80 - $30.36
9% of jobs
$30.36 - $35.91
4% of jobs
$35.91 - $41.47
7% of jobs
$41.82 is the 25th percentile. Wages below this are outliers.
$41.47 - $47.02
9% of jobs
The median wage is $52.58 / hr.
$47.02 - $52.58
17% of jobs
$52.58 - $58.14
7% of jobs
$58.14 - $63.69
14% of jobs
$65.46 is the 75th percentile. Wages above this are outliers.
$63.69 - $69.25
12% of jobs
$69.25 - $74.80
10% of jobs
$74.80 - $80.36
7% of jobs
$19
$54
$80
How much do entry level clinical sas programmer jobs pay per hour?
As of Sep 14, 2026, the average hourly pay for entry level clinical sas programmer in Delaware is $54.08, according to ZipRecruiter salary data. Most workers in this role earn between $41.63 and $68.08 per hour, depending on experience, location, and employer.
What is an entry level clinical SAS programmer?
An Entry Level Clinical SAS Programmer is responsible for programming and analyzing clinical trial data using SAS software. They assist in creating datasets, reports, and statistical outputs that comply with regulatory standards. Their work supports biostatisticians and clinical teams in pharmaceutical companies, contract research organizations (CROs), or healthcare institutions. This role requires knowledge of SAS programming, clinical research processes, and regulatory requirements such as CDISC standards. It is an excellent starting point for those looking to build a career in clinical data analysis and biostatistics.
What are the typical responsibilities of an entry level clinical SAS programmer?
Entry Level Clinical SAS Programmers are primarily responsible for writing and validating SAS code to process clinical trial data, generate tables, listings, and figures, and support statistical analysis plans. They work closely with biostatisticians, data managers, and other team members to ensure data integrity and compliance with regulatory standards. Daily tasks may involve data cleaning, programming data checks, and documenting code for reproducibility. This role offers great exposure to the clinical data lifecycle and provides a strong foundation for professional growth within clinical research and data analytics.
What are the key skills and qualifications needed to thrive as an entry level clinical SAS programmer?
To thrive as an Entry Level Clinical SAS Programmer, you need a solid understanding of SAS programming, statistics, and clinical trial processes, often supported by a degree in computer science, statistics, or a related field. Familiarity with SAS software, data management systems, and FDA or CDISC standards is highly valued, and SAS certification can be a plus. Attention to detail, strong problem-solving skills, and effective communication are key soft skills for this role. These competencies ensure high-quality data analysis, regulatory compliance, and clear collaboration across teams in pharmaceutical or clinical research settings.
What are the most commonly searched types of Clinical Sas Programmer jobs in Delaware?
The most popular types of Clinical Sas Programmer jobs in Delaware are:
What are popular job titles related to Entry Level Clinical Sas Programmer jobs in Delaware?
For Entry Level Clinical Sas Programmer jobs in Delaware, the most frequently searched job titles are:
What job categories do people searching Entry Level Clinical Sas Programmer jobs in Delaware look for?
The top searched job categories for Entry Level Clinical Sas Programmer jobs in Delaware are:
Senior Principal Biostatistician
Wilmington, DE • On-site
Incyte Corporation
• Pharmaceutical and Medicine Manufacturing • 501 - 1,000 employees501 - 1,000 employees
Full-time
Posted 7 days ago
Job description
Overview
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only).
Job Summary (Primary function)
This role is responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials and leading project teams.
Essential Functions of the Job (Key responsibilities)
• Other responsibilities as required.
• Participate in the development and enforcement of SOPs and guidelines.
• Participate in pre-IND and NDA activities.
• Participate and contribute to authoring of Clinical Development Plan.
• Assist in writing relevant sections of the clinical study report.
• Interpret study results and provide review of statistical summary reports of study results for accuracy.
• Provide guidance and support to team members in creating analysis dataset specifications and programming of tables, listings, and figures.
• Write statistical analysis plans.
• Provide statistical input to study protocols.
• Interact with members of the multidisciplinary project teams to establish project timelines.
Qualifications (Minimal acceptable level of education, work experience, and competency)
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
A global biopharmaceutical company on a mission to Solve On, Incyte follows science to find solutions for patients with unmet medical needs. Through the discovery, development, and commercialization of proprietary therapeutics, Incyte has established a portfolio of first-in-class medicines for patients and a strong pipeline of products in Hematology, Oncology and Inflammation and Autoimmunity
Headquartered in Wilmington, Delaware, Incyte has operations in North America, Europe, and Asia.
The job is based in Wilmington Delaware, US. (Minimum 3 days per week in the office. Local candidates or those willing to relocate only).
Job Summary (Primary function)
This role is responsible for processing clinical data required for statistical analysis of Phase I - III clinical trials and leading project teams.
Essential Functions of the Job (Key responsibilities)
• Other responsibilities as required.
• Participate in the development and enforcement of SOPs and guidelines.
• Participate in pre-IND and NDA activities.
• Participate and contribute to authoring of Clinical Development Plan.
• Assist in writing relevant sections of the clinical study report.
• Interpret study results and provide review of statistical summary reports of study results for accuracy.
• Provide guidance and support to team members in creating analysis dataset specifications and programming of tables, listings, and figures.
• Write statistical analysis plans.
• Provide statistical input to study protocols.
• Interact with members of the multidisciplinary project teams to establish project timelines.
Qualifications (Minimal acceptable level of education, work experience, and competency)
- PhD in Statistics/biostatistics, Working experience in pharma/biotech, hands on working experience in clinical trials
- Strong technical background for statistical methodology work
- Proficiency in using SAS to perform efficacy analyses and validate important data derivations when necessary
- Familiarity with multivariate analyses and biomarker analyses is beneficial.
- Experience in collaborating with health authorities, including discussions and negotiations in filing strategies, is highly valued. Able to effectively communicate their ideas and to manage team members in a constructive manner.
- Demonstrate ability to work autonomously in project management and decision making.
- Several years of experience in pharmaceutical/biotechnology industries and a broad knowledge of biostatistics, FDA/EMEA guidelines, and the drug development process.
- Advanced degree in statistics or equivalent experience preferred.
Disclaimer: The above statements are intended to describe the general nature and level of work performed by employees assigned to this job. They are not intended to be an exhaustive list of all duties, responsibilities, and qualifications. Management reserves the right to change or modify such duties as required.
Incyte Corporation is committed to creating a diverse environment and is proud to be an equal opportunity employer.
We Respect Your Privacy
Learn more at: http://www.incyte.com/privacy-policy
The Incyte hiring organization processes your personal data to manage your job application in order to enter into an employment relationship with you if you are the successful candidate.
During the process, you may be asked to respond to questions that will screen out your application if you do not meet certain objective criteria required by the job. You can learn more about this process here.
You may have the right to access, delete, restrict, edit, move, or object to the use of your personal data. You may also have a right to report concerns to the authority responsible for data privacy in the country where the position is based or where you live or work.
You can learn more about Incyte's data protection practices here. By accessing this link you can learn about the types of personal data we collect, how we use it, whether collection and processing is optional, sources of the personal data we process, how it is shared, where it is stored or transferred to, how long we keep it, and contact information for Incyte, Incyte's data protection officer, and your supervisory authority (if applicable).
Please contact privacy@incyte.com if you have any questions or concerns or would like to exercise your rights.
About Incyte
Sourced by ZipRecruiter
Industry
Pharmaceutical and medicine manufacturing
Company size
501 - 1,000 Employees
Headquarters location
Wilmington, DE, US
Year founded
1991