SR. CLINICALÂ SASÂ PROGRAMMER
SR. CLINICALÂ SASÂ PROGRAMMER
Employer Active
Job Alert
You will be updated with latest job alerts via email
Share
Job Alert
You will be updated with latest job alerts via email
Not Disclosed
Salary Not Disclosed
1 Vacancy
Job Description
Responsibilities:
- Perform data manipulation analysis and reporting of clinical trial data.
- Develop and maintain department/system-level macros.
- Create and review SDTM and Adam specifications.
- Create and validate SDTM data sets.
- Create and validate analysis data sets.
- Create and validate patient profiles.
- Program and generate tables figures and listings (TFLs).
- Validate and document SAS programs and outputs.
- Fulfil ad-hoc analysis requests.
- Provide other services.
Requirements:
- Bachelors degree or higher preferably in a scientific discipline such as Statistics Mathematics Computer Science or a related applicable field.
- Minimum of ten (10) years SAS programming experience in the pharmaceutical/biotech industry with extensive experience using CDISC standards.
- Ability to create source and validation programs using SAS software for SDTM datasets Adam datasets and tables figures and listings (TFLs) for multiple studies/products.
- Experience integrating data across multiple studies or drug programs.
- Expertise in developing and using system-level macro programs.
- Experience programming with SAS/GTL.
- Proficiency in Microsoft Word Excel and PowerPoint.
Additional Information :
All your information will be kept confidential according to EEO guidelines.
Remote Work :
No
Employment Type :
Contract
Employment Type
Contract
