Senior Data Analyst

24 hours ago

Salem, Tamil Nadu, India beBeeStatistical Full time ₹ 80,00,000 - ₹ 1,20,00,000
Job Description:

Sponsor-dedicated opportunity to drive innovation in patient treatment.

As a Senior Statistical Programmer, you will be embedded within one of our clients, working closely with their team to support the development of new treatments.

This is an exciting time to join our client's innovative program, 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 as fully remote.



Our Values:
  • We apply scientific rigor to reveal the full promise inherent in data.
  • We nurture intellectual curiosity and encourage everyone to approach new challenges with enthusiasm and desire for discovery.
  • We believe in collaboration and invite diversity of perspectives to create wealth of possibilities.
  • We prize innovation and seek intelligent solutions using leading-edge technology.


Responsibilities:

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 and/or responding to internal cross-functional teams and client for project specifications, status, issues or inquiries.

Performing lead duties when called upon.

Serving as team player, with willingness to go extra distance to get results, meet deadlines, etc.

Being adaptable and flexible when priorities change.



Qualifications:

Bachelor's degree in Statistics, Computer Science, Mathematics, etc.

At least 7 years of SAS programming working with clinical trial data in Pharmaceutical & Biotech industry with bachelor's degree or equivalent. At least 5 years of related experience with 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 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 manipulation, analysis and reporting of clinical trials' data.

Submissions experience utilizing define.xml and other submission documents.

Experience supporting immunology, respiratory or oncology studies would be plus.

Excellent analytical & troubleshooting skills.

Ability to provide quality output and deliverables, in adherence with challenging timelines.

Ability to work effectively and successfully in globally dispersed team environment with cross-cultural partners.

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