Send me more jobs like this

"Clinical SAS Programmer"

Keywords / Skills : "Clinical SAS Programmer"

4 - 8 years
Posted: 2019-02-26

Other Pharma
Posted On
26th Feb 2019
Job Description
Job Description:
• Good Clinical Domain knowledge understanding clinical phases and Work expr must be in clinical domain with min 2 projects (Phase I-IV).

• Create Data transfer specification by referring the eCRF, Annotation of eCRF, knowledge on Protocol.

• Create SAS datasets of clinical data from raw data; create status and efficacy datasets; create project specific

• macros and formats; load client data from other platforms; prepare data to be sent to clients.

• Create listings and Custom reports as per customer requirement.

• Knowledge on Vendor Import programmer

• Strong Technical knowledge on SAS programming, CDISC SDTM standards, Semi SDTM (Sponsor based standards).

• SAS /BASE, SAS/Advance SAS, SAS/ Macros, SAS/SQL & SAS/SAS Grid knowledge is required.

• Data listings, in accordance with approved statistical analysis plan and shell displays for clinical research studies.

• Code is to be written using Base SAS programs, SAS procedures, or standardized macros. Perform data checks

• as needed to understand structure and content of data.

• Coordinate the different project stake holder on project deliverables.

• Create and maintain Standard QC documentation and maintain the accuracy.

• Good Communication skill

About Company

IQVIA, formerly Quintiles and IMS Health, Inc., is an American multinational company serving the combined industries of health information technologies and clinical research.
Walkin for you