Data Analysis Specialist

4 days ago

Agra, Uttar Pradesh, India beBeeStatistical Full time ₹ 80,00,000 - ₹ 1,10,00,000

Job Title: Advanced Data Analyst

Sponsor-dedicated role.

As a key member of our team, you will be embedded with one of our global pharmaceutical clients, working closely with their team to drive innovation and deliver results. This is an exciting opportunity to contribute to the next generation of patient treatment and empower individuals with autonomy and ownership.

Position Overview:

As a Senior Statistical Programmer, you will utilize 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.

Key Responsibilities:

We believe in collaboration and invite diverse perspectives to create new possibilities. Our values include:

  • Applying scientific rigor to reveal data promise
  • Nurturing intellectual curiosity for new challenges
  • Collaboration and diverse perspectives
  • Innovation and intelligent solutions using leading-edge technology

How you will contribute:

Performing data manipulation, analysis, and reporting of clinical trial data, both safety and efficacy (ISS/ISE), 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

Applying strong understanding/experience of Efficacy analysis

Creating and reviewing submission documents and eCRTs

Communicating with internal cross-functional teams and client for project specifications, status, issues, or inquiries

Leading duties when called upon

Being adaptable and flexible when priorities change

Qualifications:

To succeed in this position, you will have:

  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent
  • Study lead experience, preferably juggling multiple projects simultaneously preferred
  • Strong SAS data manipulation, analysis, and reporting skills
  • Solid experience implementing the latest CDISC SDTM/ADaM standards
  • Strong QC/validation skills
  • Good ad-hoc reporting skills
  • Proficiency in Efficacy analysis
  • Familiarity with drug development life cycle and experience with manipulating, analyzing, and reporting clinical trials' data
  • Submissions experience utilizing define.xml and other submission documents
  • Excellent analytical & troubleshooting skills
  • Ability to provide quality output and deliverables within challenging timelines
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners

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