Senior Data Analyst

2 days ago

Cochin, Kerala, India beBeeStatistical Full time ₹ 15,00,000 - ₹ 20,00,000

Sponsor-dedicated role

You will be embedded within one of our pharmaceutical clients, working with the support of Cytel right behind you.

This is an exciting time to be part of a new program driving the next generation of patient treatment, where individuals are empowered to work with autonomy and ownership.

Position Overview

You will leverage 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 fully remote.

Our Values

  • We apply scientific rigor to reveal data's full promise.
  • We nurture intellectual curiosity and encourage enthusiasm for discovery.
  • We collaborate and draw on diverse perspectives to create possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.

Responsibilities

How You Will Contribute

  • Data manipulation, analysis, and reporting for clinical trial data, utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis files, and tables, listings, and figures.
  • Production and QC/validation programming.
  • Generating complex ad-hoc reports utilizing raw data.
  • Efficacy analysis application.
  • Creating and reviewing submission documents and eCRTs.
  • Communicating with internal cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Performing lead duties when called upon.
  • Serving as a team player, willing to go the extra distance to get results, meet deadlines.
  • Being adaptable and flexible when priorities change.

Qualifications

To succeed in this position, you will have:

  • A Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry.
  • Study lead experience, preferably juggling multiple projects simultaneously.
  • SAS data manipulation, analysis, and reporting skills.
  • CDISC SDTM/ADaM standard implementation experience.
  • QC/validation skills.
  • Ad-hoc reporting skills.
  • Efficacy analysis proficiency.
  • Familiarity with drug development life cycle and clinical trial data manipulation, analysis, and reporting.
  • Submission experience using define.xml and other submission documents.
  • Experience supporting immunology, respiratory, or oncology studies would be a plus.
  • Excellent analytical and troubleshooting skills.
  • Ability to provide quality output and deliverables under challenging timelines.
  • Ability to work effectively in a globally dispersed team environment.

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