PLEASE NOTE: Must be authorized to work lawfully in the United States for any employer without sponsorship. For immediate consideration, please apply.

Kelly® Science & Clinical is seeking a remote Clinical SAS Programmer for a temporary position (with potential to extend/convert) at a leading client in Thousand Oaks, CA. If you’re passionate about bringing the latest scientific discoveries to life and are ready to take the next step in your career, trust The Experts at Hiring Experts.

Pay Rate:
$65-85.00+/Hour (commensurate with experience)

Overview:
We are seeking a highly skilled Clinical SAS Programmer to join our dynamic team in the biotechnology industry. The successful candidate will be responsible for providing programming support for clinical trial data, ensuring the quality and integrity of clinical trial analysis and submissions to regulatory authorities.

Schedule:
Monday – Friday, 1^st/Day: Standard Hours (weekend work available but not required)

Responsibilities:

• Develop, test, and validate SAS programs for clinical trial data analysis and reporting.
  

• Generate and QC tables, listings, and figures (TLFs) for clinical study reports.
  

• Provide programming support for data management, data review, and ad hoc analyses.
  

• Ensure compliance with regulatory requirements (e.g., FDA, EMA) and company standards.
  

• Participate in the creation of submission documentation for regulatory filings.
  

• Collaborate with statisticians and other team members to ensure timely and accurate delivery of high-quality datasets and outputs.
  

• Perform programming and validation of data integration and data mapping as necessary.

Qualifications:

• Bachelor’s degree in Computer Science, Statistics, Mathematics, or a related field; advanced degree preferred.
  

• At least 3 years of experience as a SAS programmer in the pharmaceutical or biotechnology industry.
  

• Strong experience with SAS programming (data step, PROC SQL, macros, and statistical procedures).
  

• Demonstrated experience with Pinnacle 21 and submissions to regulatory authorities.
  

• Knowledge of CDISC standards (SDTM, ADaM) and regulatory submission requirements.
  

• Excellent problem-solving skills and attention to detail.
  

• Strong communication and collaboration abilities.

Preferred Skills:

• Exposure to clinical trials in rare diseases.
  

• Experience with other programming languages (e.g., R, Python).
  

• Familiarity with clinical data management systems (e.g., Medidata Rave, Oracle Clinical).

What Happens Next:
Once you apply, you’ll proceed to next steps if your skills and experience look like a good fit. But don’t worry – even if this position doesn’t work out, you’re still in our network. That means our team of expert Science & Clinical recruiters will have access to your profile, making your opportunities limitless.

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