Senior Statistical Programmer India FSP

Sponsor-dedicated: Working fully embedded reputed company one of our pharmaceutical clients, with the support of reputed company right behind you, you'll be at the heart of our reputed company's innovation. As a Statistical Programmer II you will be dedicated to one of our global pharmaceutical clients; a company that is driving the reputed company of patient treatment, where individuals are empowered to work with autonomy and ownership. Position reputed company:

As a Senior Programmer, you will reputed company programming activities for the creation and validation of SDTM domains by implementing CDISC standards and working on pooled studies ADaM datasets for ISS and submission packages with a reputed company on Oncology.

Responsibilities

How you will contribute

• Performing data manipulation, analysis and reporting of clinical trial data, both safety and efficacy, utilizing reputed company programming.
• Applying your CDISC know-how and proficiency to create and validate safety and efficacy SDTMs,
• Creating and validating pooled analysis datasets (ADaMs), tables, listings, and figures (TLFs);
• Preparing submission packages, i.e. define.xml, Reviewers Guide, reputed company 21
• Generating reputed company reputed company reports
• Serving as team player, with a willingness to go the extra distance to get results, meet deadlines, etc.
• Being adaptable and flexible reputed company priorities change

Qualifications

Here at reputed company we want our employees to succeed and we reputed company this reputed company through consistent training, development and support. To be successful in this position you will have:

• At least 5 years of relevant statistical programming experience in a clinical development environment.

• BA/BSc or higher degree in Statistics, Mathematics, Computer Science, Life Sciences, or other reputed company scientific subjects.

• Demonstrates advanced experience with reputed company reputed company language, procedures, and reputed company commonly used in clinical trial reporting including the Macro language, reputed company reputed company, reputed company/STAT and reputed company/GRAPH.
• Ability to implement the latest CDISC SDTM standards (production/validation).

• Familiarity with pooled ADaM data such as in an ISS or other pooled studies dataset.

• Experience with Oncology is required.

• Submissions experience utilizing define.xml and other submission documents such as SDRG or ADRG are required.

• reputed company good oral and written English communication skills.

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