Clinical Trials Data Analyst

3 days ago

Aligarh, Uttar Pradesh, India beBeeStatistical Full time ₹ 16,00,000 - ₹ 21,00,000

Job Opportunity:

Sponsor-dedicated professionals with advanced SAS programming skills and proficiency in CDISC standards (SDTM & ADaM) are sought after to support or lead Phase I-IV clinical trials.

As a Senior Statistical Programmer, you will be working fully embedded within one of our pharmaceutical clients. With the support of our team right behind you, you'll be at the heart of our client's innovation.

This is an exciting time to be part of this new program.

Our ideal candidate has at least 7 years of experience in SAS programming, preferably juggling multiple projects simultaneously, with solid knowledge in implementing the latest CDISC SDTM/ADaM standards.

We're looking for someone with strong analytical and troubleshooting skills, ability to provide quality output and deliverables, in adherence with challenging timelines.

Key Responsibilities Include:

  • Performing data manipulation, analysis and reporting of clinical trial data using SAS programming
  • Generating and validating SDTM and ADaM datasets/files, tables, listings and figures
  • Production and QC/validation programming
  • Generating complex ad-hoc reports using raw data
  • Applying strong understanding/experience of Efficacy analysis
  • 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
  • Being adaptable and flexible when priorities change

Required Skills And Qualifications:

  • Bachelor's degree in Statistics, Computer Science, Mathematics, etc.
  • At least 7 years of experience with SAS programming working with clinical trial data in the Pharmaceutical & Biotech industry
  • Study lead experience, preferably juggling multiple projects simultaneously preferred
  • Strong data manipulation, analysis and reporting skills
  • Proficiency in Efficacy analysis
  • Experience supporting immunology, respiratory or oncology studies would be a plus
  • Excellent analytical & troubleshooting skills
  • Ability to provide quality output and deliverables, in adherence with challenging timelines

Benefits:

Here at Cytel we want our employees to succeed, and we enable this success through consistent training, development and support.

You will have the opportunity to work on innovative projects with top global pharmaceutical companies, and grow your professional network.

Why This Job Is Perfect For You:

This role offers the chance to use your expertise to make a significant impact on the pharmaceutical industry.

With a strong focus on innovation and teamwork, you'll be working alongside experts who share your passion for delivering exceptional results.

Join us to discover a fulfilling career path that brings out the best in you.

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