ZipRecruiter

Log In

1

Sas Clinical Data Jobs (NOW HIRING)

SystImmune, Inc

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic ... Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Lancesoft

Senior Statistical Programmer

Irvine, CA · On-site

$75 - $98.48/hr

Base SAS * Clinical Data Interchange Standards Consortium (CDISC) Standards * Data Manipulation * SAS Macros * SAS/STAT Nice To Have * Python * R * Provide hands on statistical programming support ...

Centria Autism

Clinical Data Analyst

Farmington Hills, MI · On-site

$105K - $115K/yr

The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Familiarity with statistical analysis tools (R, Python, or SAS) is a plus. * Working knowledge of ...

Centria Autism

Clinical Data Analyst

Farmington Hills, MI · On-site

$105K - $115K/yr

The Clinical Data Analyst partners with clinical leadership, payor relations, and operations to ... Familiarity with statistical analysis tools (R, Python, or SAS) is a plus. * Working knowledge of ...

Systimmune

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating ...

SystImmune, Inc

Clinical Data Analyst, Spotfire

Redmond, WA · On-site

$90K - $130K/yr

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial data standards (CDISC SDTM, ADaM), experience with TLF generation preferred. * Experience integrating ...

CICONIX, LLC

SAS Programmer

Fort Detrick, MD

SAS Programmer About CICONIX: CICONIX LLC is a Veteran Owned Small Business specializing in ... Develop statistical programming specifications (clinical data) and other statistical programs used ...

Viz.ai

Clinical Data Manager

$127K - $182K/yr

... SQL, SAS, Python, R). * You excel in strategic thinking and operational execution, adept at ... Required * 5-7+ years in clinical research/RWE data management with hands-on database build ...

next page

Showing results 1-20

All JobsSas Clinical Data Jobs

Sas Clinical Data information

See salary details

$19

$54

$80

How much do sas clinical data jobs pay per hour?

As of Jun 11, 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 6% Locum Tenens, 37% As Needed, 9% Full Time, 9% Part Time, 6% Temporary, and 33% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $112,399 per year, or $54 per hour.
Clinical Data Associate

Clinical Data Associate

SystImmune, Inc

Redmond, WA • On-site

$75K - $95K/yr

Full-time

Medical, Dental, Vision, Retirement, PTO

Posted 7 days ago

Job description

SystImmune is a leading and well-funded clinical-stage biopharmaceutical company located in Redmond, WA and Princeton, NJ. It specializes in developing innovative cancer treatments using its established drug development platforms, focusing on bi-specific, multi-specific antibodies, and antibody-drug conjugates (ADCs). SystImmune has multiple assets in various stages of clinical trials for solid tumor and hematologic indications. Alongside ongoing clinical trials. SystImmune has a robust preclinical pipeline of potential cancer therapeutics in the discover and IND-enabling stages, representing cutting-edge biologics development. We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
The Clinical Data Associate (CDA) supports the Clinical Data Manager in executing data management activities across clinical trials, with a primary focus on Phase 3 and other large-scale studies. The CDA will gain hands-on experience across the full DM lifecycle while working under the guidance of senior data management staff.
This role is full-time onsite in Redmond, WA. Please note that SystImmune plans to relocate to a new facility in Bothell, WA in the fall.
Responsibilities:
  • Support the CDM in day-to-day data management activities across study start-up, maintenance, and close-out, including tracking open queries and data cleaning timelines.
  • Assist in the development and review of DM documents such as Data Management Plans, CRF Completion Guidelines, and data review plans using established templates and standards.
  • Perform data review activities including query generation, query resolution follow-up, and non-system edit check output review under CDM oversight.
  • Assist with SAE reconciliation and non-CRF data reconciliation activities, escalating issues to the CDM as appropriate.
  • Support medical coding activities using MedDRA and WHO Drug dictionaries, coordinating with the CDM and CRO for medical review.
  • Run and review SAS and/or R programs and data listings as directed; assist in troubleshooting basic programming errors under CDM guidance.
  • Perform UAT (User Acceptance Testing) of EDC systems and edit checks per provided specifications and test scripts.
  • Assist in tracking and coordinating CRO/vendor deliverables, flagging risks or delays to the CDM.
  • Contribute to data quality monitoring by reviewing metrics reports and flagging trends or anomalies to the CDM.
  • Support database lock activities by assisting with lock checklists, outstanding query resolution, and coordination tasks.
  • Participate in the development and review of DM SOPs and process improvement initiatives.
  • All other duties as assigned.

Qualifications:
  • BA or BS in life sciences, health informatics, or a related field.
  • 1-3 years of relevant clinical data management or clinical research experience; equivalent internship or co-op experience in a clinical or pharma setting will be considered.
  • Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred.
  • SAS, Python, and R programming knowledge is a plus.
  • Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines preferred; willingness to develop deep knowledge required.
  • Detail-oriented with strong organizational and time management skills.
  • Effective written and verbal communication skills; ability to work cross-functionally.
  • Eagerness to learn in a fast-paced, clinical-stage biopharmaceutical environment.
  • Oncology experience or interest a plus.

Compensation and Benefits:
The expected base salary range for this position is $75,000 - $95,000 annually. Actual compensation will be based on a variety of factors, including but not limited to a candidate's level qualifications, experience, and skills.
While most offers typically fall within the low to mid-point of the range, we may extend an offer toward the higher end for exceptional candidates whose background and expertise exceeds the requirements of the role.
SystImmune is a leading and well-funded biotech company with a bright future. We offer an opportunity for you to learn and grow while making significant contributions to the company's success. SystImmune offers a comprehensive benefits package including: 100% paid employee premiums for medical/dental/vision, also STD, LTD, a 401(k) plan with a 50% company match of up to 3% and a vesting schedule of only 5 years, 15 PTO days per year, sick leave, plus 11 paid holidays and MORE.
We offer an opportunity for you to learn and grow while making significant contributions to the company's success.
SystImmune is an Equal Opportunity Employer. We welcome diverse talent and encourage all qualified applicants to apply.

Apply