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Senior Statistical Programmer FSP at Cytel
, , India -
Full Time

Start Date

Immediate

Expiry Date

21 Aug, 26

Salary

0.0

Posted On

23 May, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

SAS Programming, CDISC SDTM, CDISC ADaM, Clinical Trial Data, Study Lead Experience, QC/Validation, Ad-hoc Reporting, Efficacy Analysis, Define.xml, Drug Development Life Cycle, Analytical Skills, Troubleshooting

Industry

Pharmaceutical Manufacturing

Description
Sponsor-dedicated:   Working fully embedded within one of our pharmaceutical clients, with the support of Cytel right behind you, you'll be at the heart of our client's innovation. As a Senior Statistical Programmer you will be dedicated to one of our global pharmaceutical clients; a company that is driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership. This is an exciting time to be a part of this new program. Position Overview:  As a Senior Statistical Programmer, you will leverage your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role can be performed as fully remote. Our values * We believe in applying scientific rigor to reveal the full promise inherent in data. * We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and the desire for discovery. * We believe in collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. * We prize innovation and seek intelligent solutions using leading-edge technology.
Responsibilities
The Senior Statistical Programmer will lead or support Phase I-IV clinical trials by leveraging advanced SAS programming and CDISC standards. They will be embedded within a pharmaceutical client to drive innovation in patient treatment through data analysis and reporting.