Clinical SAS Programmer
Clinical SAS 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
- 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 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 eCRF SDTM and ADaM datasets specifications for datasets programming.
- Provides programming support for adhoc analysis.
- Identifies problems and develops global tools that increase the efficiency and capacity of the Statistical Programming group (e.g. macros or graphical user interface applications).
Requirements:
- 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.
Employment Type
Full-time
