Clinical SAS Programmer
Clinical SAS Programmer
Posted on :
25-07-2025
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1 Vacancy
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Job Description
Responsibilities:
- Effectively designs and codes SAS programs using BASE/SAS SAS/STAT SAS/GRAPH and SAS MACROS for assigned clinical projects(s).
- Produces and delivers CDISC and regulatory compliant SDTM and ADaM standard datasets.
- Creates and validates tables figures and listings (TFLs) in a timely and high-quality fashion consistently meeting objectives of the study and regulatory requirements.
- Provides input in the design and development of case report forms and clinical databases.
- Performs quality control checks/validation of SAS code and output produced by other Statistical Programmers for SDTM datasets ADaM datasets and TFLs.
- Programs for quality checks for clinical study raw data and report the findings to Data Management.
- Provides input in the design and development of case report forms and clinical study databases.
- Reviews or author aCRF SDTM and ADaM datasets specifications for datasets programming.
- MS in Statistics Computer Science or a related field with at least 3 years or BS in Statistics Computer Science or a related field with at least 5 years.
- Experience in providing statistical programming support to early and late phase clinical trials.
- Excellent skills in SAS programming and statistical reporting.
- Knowledge of CDISC standards for SDTM and ADaM and FDA electronic data submission requirements.
- Familiarity with FDA and ICH regulations and guidelines.
- Excellent problem-solving skills.
- Good written and verbal communication skills and organizational and documentation skills.
- Ability to work on a multidisciplinary team that may include Biostatistics Medical Directors Data Management Medical Writing Pharmacovigilance Clinical Operations Medical Affairs etc.
- Ability to prioritize and multi-task effectively.
- Demonstrated positive attitude and the ability to work well with others.
Employment Type
Full-time
Key Skills
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