Senior Data Analyst

2 days ago

Mysore, Karnataka, India beBeeStatistical Full time ₹ 15,00,000 - ₹ 20,00,000

We are seeking a skilled Senior Data Analyst to join our team.

This is an exciting opportunity for a seasoned professional to take on a leadership role and make a meaningful impact in the pharmaceutical industry. As a Senior Statistical Programmer, you will be responsible for leveraging your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials.

The ideal candidate will have a strong background in statistics and experience working with clinical trial data in the Pharmaceutical & Biotech industry. They will be proficient in performing data manipulation, analysis and reporting, as well as generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).

In addition to technical skills, the successful candidate will possess excellent analytical and troubleshooting skills, with the ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

We value collaboration and invite a diversity of perspectives, drawing on a variety of talents to create a wealth of possibilities. Our team is passionate about applying scientific rigor to reveal the full promise inherent in data, and we encourage everyone to approach new challenges with enthusiasm and the desire for discovery.

Responsibilities
  • Data manipulation, analysis, and reporting of clinical trial data, utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures (TLFs).
  • Production and QC/validation programming.
  • Generating complex ad-hoc reports utilizing raw data.
  • Efficacy analysis.
  • Creating and reviewing submission documents and eCRTs.
  • Communicating with internal cross-functional teams and clients for project specifications, status, issues or inquiries.
Requirements
  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry.
  • Study lead experience, preferably juggling multiple projects simultaneously.
  • Solid experience implementing the latest CDISC SDTM / ADaM standards.
  • Strong QC/validation skills.
  • Familiarity with drug development life cycle and experience with the manipulation, analysis and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.

Benefits:

  • Consistent training, development, and support.
  • A willingness to go the extra distance to get results, meet deadlines, etc.
About Us

We are a company dedicated to empowering individuals to succeed through consistent training, development, and support. We believe in collaboration, inviting a diversity of perspectives, and drawing on a variety of talents to create a wealth of possibilities.

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