Statistical Programmer(Clinical Reserch) Global MNC : CTC 20LPA Hurry!

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Statistical Programmer!!!

We are hiring for:

Statistical Programmer up to 20 lpa ctc

Experience Level: 5 to 15 years

Location- Mumbai, Pune, Noida, Bangalore

We are looking for a skilled Senior Statistical Programmer I / II to join our team at Icon Pharmaceuticals. The ideal candidate will have a strong background in statistical programming and analysis, with excellent problem-solving skills and attention to detail..

Key Responsibilities:

Develop and maintain complex statistical models and algorithms to support business intelligence initiatives.

Collaborate with cross-functional teams to design and implement data visualizations and reports.

Conduct statistical analysis and interpretation of large datasets to inform business decisions.

Design and develop predictive models to drive business growth and improvement.

Ensure compliance with regulatory requirements and industry standards in all aspects of statistical programming.

Provide technical guidance and support to junior team members on statistical programming best practices.

Job Requirements

Strong understanding of statistical concepts and techniques, including regression analysis and time series forecasting.

Proficiency in statistical software packages such as SAS or R, with experience in programming languages like Python or SQL.

Excellent communication and interpersonal skills, with the ability to work effectively in a team environment.

Strong problem-solving skills, with the ability to analyze complex data sets and identify trends and patterns.

Ability to prioritize multiple tasks and deadlines in a fast-paced environment.

Strong attention to detail, with a focus on delivering high-quality results and meeting project timelines.

Required Qualifications:

Bachelors or Masters degree in Statistics, Computer Science, or a related field

5+ years of SAS programming experience in clinical research or pharmaceutical industry

Strong hands-on experience with ADaM, TFLs, eSubmissions, and integrated analysis

Creation and validation of ISS and ISE reports

Deep understanding of CDISC standards, regulatory compliance, and submission requirements

Prior experience in oncology, neuroscience, or immunology domains preferred

Proven leadership capabilities in managing cross-functional and global teams

Excellent communication, project management, and problem-solving skills

Preferred Tools & Skills:

SAS (Base, Macro, STAT, Graph)

Creation and validation of ISS and ISE reports

Familiarity with SDTM/ADaM IG, FDA submission standards
Creation and validation of ISS and ISE reports

Understanding of regulatory submission formats (eCTD)

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