Senior SAS Programmer

Boston, Massachusetts

Come Join Our Growing Team!

We are looking for a Senior SAS Programmer to join our team.

What The Job Entails:

  • Perform SAS data processes and analysis programming.
  • Works with Statistician and Statistical programmer to assure results are consistent with expectations, and quality control (QC) procedures are followed.
  • Works collaboratively to meet study deliverables and timelines for statistical data analysis and reporting.
  • Plans and carefully documents differences between programming results between program developer and Statistical QC programmer.
  • Provided programming support on ISS/ISE and post-submission activities.
  • Provide flexible and rapid response to programming requests.
  • Ensure the consistency and adherence to standards within the project.
  • Confirms that tracking sheets are current for projects, and confirm that results are consistent with earlier generated results.
  • Maintain up-to-date study documentation.
  • Develop, program, test and maintain computer validation/edit checks in SAS.
  • Validate peer programming. Provide technical expertise and support to Data Management team.
  • Routinely interface with cross-functional team members.
  • Participate in regular team meetings and provide input when appropriate.
  • Participate in the programming processes from study start up to database lock. Managing project priorities and timelines.
  • Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.
  • BS degree or higher in programming or statistics.
  • SAS Experience in Pharmaceutical or equivalent: >=3 years, Oncology experience preferred.
  • Have good knowledge of statistical terminology, clinical data structure, clinical tests, medical terminology, regulatory standards and protocol designs.
  • Strong SAS programming / Macros development / SAS graphs skills.
  • Excellent oral and written skills for cross-site and cross-function collaboration.
  • Dependable, motivated, focused and detail orientated.
  • Ability to take direction as needed and work independently on project when necessary.
  • Capable of managing time effectively and adhering to timelines and project schedule Complementary Skills.
  • Working knowledge of SAS modules and utilities.
  • Ability to develop routines using the SAS Macro Language.
  • Understanding of biotech industry regulatory requirements.
  • Ability to use Microsoft Office tools: Word, Excel, PPT, etc.

LGBTQ Inclusion Jobs

Gain Access

Add Your Resume

Add your resume to our resume database that can be searched by employers looking to hire!

Job Alerts

Stay up to date with job alerts! Customize your alerts based on a specific area, category and receive weekly updates!

Sign up now to gain access!

More Pharmaceuticals jobs

Gaithersburg, Maryland
Posted about 18 hours ago
Otsuka Pharmaceutical
Rockville, Maryland
Posted 24 minutes ago
Otsuka Pharmaceutical
Princeton, New Jersey
Posted 24 minutes ago
View Pharmaceuticals jobs ยป

Share Inclusion Job

Senior SAS Programmer is also posted to sites within our Inclusion Job Network.

Disability inclusion jobs logo
Asian inclusion jobs logo
Black inclusion jobs logo
Diversity inclusion jobs logo
LGBTQ inclusion jobs logo
Seniors inclusion jobs logo
Women inclusion jobs logo
Hispanic inclusion jobs logo