Experience : 3 – years
Requirements :
Task Info :
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
College Preference : no-bar
Min Qualification : ug
Skills : sas, sql
Location : Mumbai
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