Icon Clinical Research
Work as DIS SAS/DIS SAS Lead Programmer
About company,
"At ICON, it's our People that set us Apart"
ICON is a global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries. We specialize in the strategic development, management and analysis of programs that support Clinical Development – from compound selection to Phase I - IV clinical studies
ICON enjoys a strong reputation for quality and is focused on staff development. We make it our mission to attract the most diverse and creative minds into the business and we continually strive to provide opportunities for our people to excel, grow and build a great career. We understand that our greatest asset is the skills and talents of our people and they are truly what set us apart.
Description:
Role Responsibility
The Biostatistics Department is responsible for the statistical aspects of clinical trials, including experimental design, designing and implementing standardized clinical data solutions, statistical analysis/programming, and reporting.
Additional Responsibilities :
* Development and delivery of loading external data
* Development and delivery of observational datasets to Sponsors and ICON Biostatistics.
* Development and delivery of CDISC compliant and sponsor defined data structures.
* Development and delivery of sponsor defined data management listings/reports
* Contributes to the creation of study level documentation and files according to departmental policy and regulatory requirements.
* Liaison with Data Management and Biostatistics on database specifications, timelines and quality requirements.
Experience and Qualification
* Appropriate computer-related qualification or equivalent
* Understanding of data structures is required as well as a basic understanding of the development and use of standard programs.
* Must work independently as well as part of a team and have good problem solving skills, attention to detail, verbal and written communications skills.
Desired Profile:
Must have 3-7 working years experience in CDISC modules using SDTM, AaDM etc.
Additional Information:
Experience: 3-7 Years
Industry Type: Pharma/ Biotech/Clinical Research
Location: Chennai
Education: B.Pharm
Ref Code: C205
For Apply/ send your resum, Nilamadhab.Mahapatra@iconplc.com
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