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

Start Date

Immediate

Expiry Date

09 Sep, 26

Salary

0.0

Posted On

11 Jun, 26

Experience

5 year(s) or above

Remote Job

Yes

Telecommute

Yes

Sponsor Visa

No

Skills

SAS Programming, CDISC Standards, SDTM, ADaM, Define.xml, Clinical Trial Methodologies, FDA/ICH Regulation, Regulatory Submissions, Leadership, R, Python, Java, Shiny, Markdown, Unix/Linux, Git

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 Principal 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:  This position reports to the Director, Biostatistics and Programming in the FSP Services business unit in Cytel.  The Principal Statistical Programmer works independently with only concept level instruction and very little supervision, tracks progress, and provides expert technical support to team members. We are looking for a highly experienced senior statistical programmer who will work on clinical development programs on different therapeutic areas and participate in overseeing CRO programmers to ensure that data summaries are delivered in a consistent, high-quality manner. This individual will be responsible for implementing all reporting and analysis activities for the Sponsor clinical trials.
Responsibilities
The Principal Statistical Programmer will implement reporting and analysis activities for sponsor clinical trials while providing expert technical support to team members. They will also oversee CRO programmers to ensure high-quality and consistent delivery of data summaries.