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"Clinical SAS Programmer"

Keywords / Skills : "Clinical SAS Programmer"

4 - 8 years
Posted: 2019-02-26

Industry
Pharmaceutical
Function
Pharmaceutical/Biotechnology
Role
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.
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