Advanced Clinical Data Analyst

1 week ago

Davangere, Karnataka, India beBeeStatistical Full time ₹ 15,00,000 - ₹ 25,00,000
Job Opportunity:

As a seasoned professional, you will play a pivotal role in driving innovation within a renowned pharmaceutical client. This is an exceptional opportunity to be at the forefront of patient treatment and empowerment.

**Position Overview:**

You will leverage your advanced SAS programming skills and expertise in CDISC standards (SDTM & ADaM) to support or lead one or more Phase I-IV clinical trials. This role offers flexibility and can be performed remotely.

**Our Values:**
  • We apply scientific rigor to unlock data's full potential.
  • We foster intellectual curiosity and encourage individuals to approach challenges with enthusiasm and a desire for discovery.
  • We believe in collaboration, embracing diverse perspectives to create possibilities.
  • We prize innovation, seeking intelligent solutions through leading-edge technology.

**Responsibilities:**
  • Performing data manipulation, analysis, and reporting of clinical trial data, utilizing SAS programming.
  • Generating and validating SDTM and ADaM datasets/analysis 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 regarding project specifications, status, issues, or inquiries.
  • Performing lead duties when called upon.
  • Serving as a team player, willing to go the extra distance to achieve results, meet deadlines, etc.
  • 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, or a related field.
  • 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 managing multiple projects simultaneously.
  • 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 cycles and experience manipulating, analyzing, and reporting clinical trial data.
  • Submissions experience using define.xml and other submission documents.
  • Experience supporting immunology, respiratory, or oncology studies would be beneficial.
  • Excellent analytical and troubleshooting skills.
  • Ability to provide quality output and deliverables, adhering to challenging timelines.
  • Ability to work effectively and successfully in a globally dispersed team environment with cross-cultural partners.

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