← Back to Job Listings
Celerion logo

SAS Data Analyst - Clinical Programming

Celerion
United States of AmericaFull Time5d

Job Summary

Celerion is seeking a full-time SAS Data Analyst - Clinical Research to join their Data Management and Biometrics team. The primary responsibilities of this position include developing, maintaining, and processing SAS programs for clinical research studies, assisting with complex projects, performing peer QC functions, and ensuring compliance with study protocols. As a member of the team, you will work on moderately complex studies that create standard and customized analysis data sets, statistical analyses, and data listings. You will also assist Senior SAS Data Analysts and Biostatisticians with complex projects and ensure compliance with department procedures. Celerion values integrity, trust, teamwork, and respect, and is an equal opportunity employer. The ideal candidate has a Bachelor's degree in Statistics, Mathematical Science, Physics, or Computing, 1+ years of SAS programming experience, and excellent interpersonal skills.

Celerion is committed to swift, exceptional clinical research through translational medicine.  Every day, we use our experience, agility, and innovative research strategies to help get drugs to market faster.  

Are you looking for an opportunity to support a business creating life-saving treatments? If so, we can't wait to meet you!

Celerion is seeking a full-time SAS Data Analyst - Clinical Research to join our Data Management and Biometrics team and provide SAS statistical support to the project team for analysis and reporting of clinical data in early stage clinical research studies. The primary responsibilities of this position are:

• Independently develop, maintain and process SAS programs for moderately complex studies that create Standard and/ or customized:  analysis data sets, statistical analyses, data listings, edit checks (clinical), tables, figures and electronic data transfers. 

• Assist Senior SAS Data Analysts and Biostatisticians with complex projects. 

• Perform peer QC functions for output from studies. 

• Ensure compliance with study protocol and department procedures.

Knowledge/Skills/Education/Licenses

  • Minimum of Bachelor's Degree in Statistics, Mathematical Science, Physics or Computing.

  • 1 + years of SAS® programming experience in a CRO or Pharmaceutical industry

  • Competent in base SAS, SAS macros, SAS/STAT and in debugging SAS programs

  • Experience applying CDISC requirements to generate ADaM datasets and supporting material such as define.xml and Reviewer's Guides

  • Excellent interpersonal skills required.

  • Demonstrated problem solving and decision making skills required.

  • Demonstrated ability to work with team required.

We require a Bachelor's degree in Statistics, Mathematical Science or Computer Science with 3+ year of SAS programming experience preferably in clinical trials OR an advanced degree in Statistics or related field. Additionally, we require excellent interpersonal skills, ability to work with a team and demonstrated problem-solving skills.

Celerion Values:       Integrity   Trust   Teamwork   Respect

Celerion is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, national origin, age, sexual orientation, gender identity, genetic information, marital status, qualified protected veteran status, or disability.