Details:

           Job Description and Responsibilities

Provide advanced technical expertise as part of a team to develop andmaintain clinical systems to meet internal and external client needs. Plan andcoordinate database design and development for local, regional, ortransnational use. Provide leadership to the Clinical Data Programmingdepartment in the area of technical expertise.

RESPONSIBILITIES

 Good Clinical Domain knowledge understanding clinical phases and Workexpr must be in clinical domain  (PhaseI-IV).

 Create Data transfer specificationby referring the eCRF, Annotation of eCRF, knowledge on Protocol.

Create SAS datasets of clinical data from raw data; create status andefficacy datasets; create project specific macros and formats; load client datafrom 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, SemiSDTM (Sponsor based standards).

SAS /BASE, SAS/Advance SAS, SAS/ Macros, SAS/SQL & SAS/SAS Gridknowledge is required.

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

Code is to be written using Base SAS programs, SAS procedures, orstandardized macros. Perform data checks as needed to understand structure andcontent of data.

Coordinate the different project stake holder on project deliverables.

Create and maintain Standard QC documentation and maintain the accuracy.

Good Communication skill

 SKILLS AND ABILITIES

 Excellent knowledge or Clinical SAS Programming.

Solid understanding of clinical drug development process

Excellent organizational, communication, and technical database skills

Abilityto establish and maintain effective working relationships with coworkers,managers and clients

Min. Qualification:

ug

Skills Required:

sas, sql