Senior Clinical Data Analyst

11 hours ago

Pune, Maharashtra, India beBeeDataAnalysis Full time ₹ 15,00,000 - ₹ 25,00,000
About the Role

As a Senior Clinical Data Analyst, you will be working closely with our client to drive innovation in patient treatment.

You'll be responsible for leveraging your advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) to support or lead Phase I-IV clinical trials.

This is an exciting opportunity to work on cutting-edge projects and contribute to the development of new treatments.

Key Responsibilities
  • Perform data manipulation, analysis, and reporting of clinical trial data using SAS programming.
  • Generate and validate SDTM and ADaM datasets/analysis files, and tables, listings, and figures.
  • 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 cross-functional teams and clients for project specifications, status, issues, or inquiries.
  • Lead duties when called upon.
Requirements

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 working with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree or equivalent. At least 5 years of related experience with a master's degree or above.
  • 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 the manipulation, analysis, and reporting of clinical trials' data.
  • Submissions experience utilizing define.xml and other submission documents.
  • Excellent analytical & troubleshooting skills.
  • Ability to provide quality output and deliverables, in adherence with challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.
What We Offer

This role offers the opportunity to work on high-profile projects and contribute to the development of new treatments. You will have the chance to work with a talented team and develop your skills in a dynamic environment.

The ideal candidate will have a strong background in SAS programming and experience working with clinical trial data. If you are a motivated and detail-oriented individual who is passionate about making a difference in patient treatment, we encourage you to apply.

About Us

We are a leading provider of data analysis services to the pharmaceutical industry. Our team of experts has extensive experience working with clinical trial data and is dedicated to delivering high-quality results.

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