This includes, but is not limited to, assistance with designing clinical research studies, writing ... such as SAS, R, Stata, and SPSS. The knowledge of other computer programs such as EndNote ...
This includes, but is not limited to, assistance with designing clinical research studies, writing ... such as SAS, R, Stata, and SPSS. The knowledge of other computer programs such as EndNote ...
Biostatistician - Research
Wilmington, DE · On-site
This includes, but is not limited to, assistance with designing clinical research studies, writing ... such as SAS, R, Stata, and SPSS. The knowledge of other computer programs such as EndNote ...
Biostatistician - Research
Wilmington, DE · On-site
This includes, but is not limited to, assistance with designing clinical research studies, writing ... such as SAS, R, Stata, and SPSS. The knowledge of other computer programs such as EndNote ...
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?
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:
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For Entry Level Clinical Sas Programmer jobs in Delaware, the most frequently searched job titles are:
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The top searched job categories for Entry Level Clinical Sas Programmer jobs in Delaware are:

Full-time
Posted 20 days ago
Nemours Children's Health rating
8.1
Based on 87 frontline employees who took The Breakroom Quiz
65th of 893 rated healthcare providers
Job description
This is a Remote position. Applicants must reside in one of the following states: Alabama, Colorado, Delaware, the District of Columbia, Florida, Georgia, Illinois, Maryland, Missouri, New Jersey, New York, North Carolina, Ohio, Pennsylvania, South Carolina, Tennessee, Texas, and Virginia.
Nemours is seeking a Biostatistician. The Biostatistician reports to and assists the Nemours Anesthesia and Surgical Outcomes Center (NASOC) in providing in-depth statistical expertise for clinicians and researchers from conception through to the conclusion of research studies. This includes, but is not limited to, assistance with designing clinical research studies, writing statistical sections of research proposals, calculating sample size and power, managing, analyzing and interpreting clinical data and databases, and authoring statistical analysis results for clinical study reports and manuscripts. The Biostatistician also participates in educational and training activities through workshops and one-on-one interactions to enhance clinician/researcher's understanding of the principles of statistics and design.
The Biostatistician is required to have sound knowledge of statistical principles and strong skills in computational methods to perform complex data manipulation and analysis using major statistical software packages such as SAS, R, Stata, and SPSS. The knowledge of other computer programs such as EndNote, Smartsheets, and PASS will be a plus. The Biostatistician is expected to possess a positive attitude, be detail-oriented, and be able to interact and explain statistical results to researchers/investigators to promote teamwork in a multidisciplinary research team setting throughout the organization.
Primary Responsibilities
1. Interact independently and with the NASOC in interactions with clinical investigators, physicians, and other scientists to provide study design and statistical and programming support from the hypothesis generation phase through dissemination of results of a study.
2. Perform power and sample size calculations, generate randomization lists and write statistical methodology section for inclusion in study protocols/proposals.
3. Perform complex data manipulation and assist investigators in setting up data for analyses.
4. Carry out statistical analyses with highest level of accuracy and present results to investigators as necessary.
5. Assist in maintenance of statistical software and systems used by the NASOC.
6. Write scripts, programs, and SQL queries to assist self and others in data processing
7. Author statistical section of the research proposal and manuscript
Qualifications
- Master's degree required
- At least 1 year of experience
What Nemours Children's Health employees say
Pay
Benefits
Hours and flexibility
Workplace
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About Nemours
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As one of the nation's leading pediatric health care systems, Nemours is committed to providing all children with their best chance to grow up healthy. We offer integrated, family-centered care to more than 300,000 children each year in our pediatric hospitals, specialty clinics, primary care practices, and school-based health centers in Delaware, Florida, Maryland, New Jersey and Pennsylvania. Nemours strives to ensure a healthier tomorrow for all children - even those who may never enter our doors - through our world-changing research, education and advocacy efforts.
Industry
Health care and social assistance and hospitals
Company size
1,001 - 5,000 Employees
Headquarters location
Jacksonville, FL, US