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Sas Clinical Data Jobs (NOW HIRING)

Omni Inclusive

SAS Clinical Developer

Rahway, NJ · On-site

SDTM/Clinical SAS 1. Must have 6-8 years of experience in the clinical domain 2. Strong knowledge of SDTM 3. Create advanced SAS macros, templates, and utilities for efficient data processing 4. Act ...

Yochana

Clinical SAS Developer:

Passaic, NJ · On-site

Job Title Must have 6-8 yrs of exp in clinical domain Strong knowledge of SDTM Create advanced SAS macros, templates, and utilities for efficient data processing Act as the primary programming point ...

E-Solutions

SDTM/Clinical SAS

Rahway, NJ · On-site

Must have 6+ yrs of exp in clinical domain 2.Strong knowledge of SDTM 3 ... Create advanced SAS macros, templates, and utilities for efficient data processing 4.Act as the ...

Cynet Systems

Clinical SAS Developer

North Wales, PA · On-site

$43 - $48/hr

Create advanced SAS macros, templates, and utilities for efficient data processing. * Act as the primary programming point of contact for biostatisticians and study teams. * Perform peer review of ...

CYNET SYSTEMS

Clinical SAS Developer

Upper Gwynedd, PA · On-site

$43 - $48/hr

Create advanced SAS macros, templates, and utilities for efficient data processing. * Act as the primary programming point of contact for biostatisticians and study teams. * Perform peer review of ...

Diverse Lynx

SAS Viya developer

Raleigh, NC · On-site

Role - SAS Viya developer Location - Raleigh NC (Onsite) Exp need - 15+ years * We are seeking a ... The ideal candidate will lead end-to-end clinical data workflows, regulatory submissions, and ...

Systimmune

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It ... Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as ...

SystImmune, Inc

Clinical Data Manager

Redmond, WA · On-site

$100K - $170K/yr

SystImmune Inc. is a clinical-stage biopharmaceutical company located in Redmond, WA. It ... Program SAS and/or R Non-System Edit Checks/Back-end checks and SAS and/or R Data Listings as ...

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Sas Clinical Data information

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How much do sas clinical data jobs pay per hour?

As of Jul 5, 2026, the average hourly pay for sas clinical data in the United States is $54.04, according to ZipRecruiter salary data. Most workers in this role earn between $41.59 and $68.03 per hour, depending on experience, location, and employer.

What are some common challenges faced by SAS Clinical Data professionals when working with large clinical trial datasets?

SAS Clinical Data professionals often encounter challenges such as handling missing or inconsistent data, ensuring data integrity, and adhering to strict regulatory requirements. Managing large and complex datasets requires strong attention to detail and effective communication with clinical research teams to clarify data discrepancies. Additionally, tight project deadlines and evolving study protocols can make prioritizing tasks and maintaining high data quality demanding. Collaborating closely with biostatisticians and data managers is essential for successful data cleaning, validation, and analysis.

What are the key skills and qualifications needed to thrive as a SAS Clinical Data Analyst, and why are they important?

To thrive as a SAS Clinical Data Analyst, you need a solid background in statistics, data management, and clinical research, typically supported by a degree in life sciences, statistics, or a related field. Proficiency in SAS programming, knowledge of CDISC standards (SDTM/ADaM), and familiarity with clinical trial data systems such as EDC are essential. Strong attention to detail, problem-solving abilities, and effective communication skills set outstanding analysts apart. These competencies ensure accurate data analysis, regulatory compliance, and clear reporting, all critical for successful clinical trials.

What are SAS Clinical Data professionals?

SAS Clinical Data professionals are experts who use SAS (Statistical Analysis System) software to manage, analyze, and report clinical trial data in the pharmaceutical, biotechnology, and healthcare industries. They play a key role in ensuring the accuracy, integrity, and regulatory compliance of clinical data. Their work involves data cleaning, manipulation, statistical analysis, and the preparation of reports for regulatory submissions. These professionals often collaborate with clinical researchers, statisticians, and regulatory teams to support drug development and approval processes.

What is the difference between Sas Clinical Data vs Clinical Data Analyst?

AspectSas Clinical DataClinical Data Analyst
Required CredentialsExperience with SAS, biostatistics, clinical research certificationsDegree in life sciences, data analysis skills, some SAS knowledge
Work EnvironmentPharmaceutical companies, CROs, clinical research settingsHealthcare organizations, research institutions, biotech firms
Employer & Industry UsagePrimarily in clinical trial data managementBroader data analysis in healthcare and research

While both roles involve handling clinical data, Sas Clinical Data specialists focus on managing and analyzing clinical trial data using SAS software, often requiring specific certifications. Clinical Data Analysts may work across various healthcare settings, utilizing a broader range of data tools. Understanding these differences helps in choosing the right career path or job search focus.

More about Sas Clinical Data jobs
What job categories do people searching Sas Clinical Data jobs look for? The top searched job categories for Sas Clinical Data jobs are:
Sas Clinical Data jobs near you
Infographic showing various Sas Clinical Data job openings in the United States as of June 2026, with employment types broken down into 4% Full Time, and 96% Part Time. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.

SAS Clinical Developer

Omni Inclusive

Rahway, NJ • On-site

Other

Posted 12 days ago

Job description

Job Title

Primary & Secondary Skill: SDTM/Clinical SAS

1. Must have 6-8 years of experience in the clinical domain

2. Strong knowledge of SDTM

3. Create advanced SAS macros, templates, and utilities for efficient data processing

4. Act as the primary programming point of contact for biostatisticians and study teams

5. Perform peer review of code and documentation for accuracy and traceability

6. Review CRF (Case Report Form) annotations and data specifications

7. Ensure compliance with CDISC standards (SDTM/ADaM) and FDA/ICH guidelines

Skill:

1. Extensive programming experience in a clinical trial environment (CRO/Pharma)

2. Expertise in SAS/BASE, SAS/STAT, and SAS/MACRO

3. In-depth knowledge of CDISC standards and regulatory submission requirements

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