Statistical Data Scientist Lead

3 weeks ago


Chennai, Tamil Nadu, India Pfizer Full time
Job Summary

We are seeking a highly skilled Statistical Data Scientist to join our team at Pfizer. The successful candidate will be responsible for leading the development and implementation of statistical programming solutions to support our clinical trials and research initiatives.

This role requires a strong background in statistical programming, data analysis, and software development, as well as excellent communication and collaboration skills. The ideal candidate will be able to work independently and as part of a team, with a focus on delivering high-quality results and contributing to the success of our organization.

  • This role requires a strong background in statistical programming, data analysis, and software development.
  • Excellent communication and collaboration skills are essential for success in this role.
  • The ideal candidate will be able to work independently and as part of a team.
  • Delivering high-quality results and contributing to the success of our organization are key responsibilities.
ResponsibilitiesKey Responsibilities

Some of the key responsibilities of this role include:

  • Developing and implementing statistical programming solutions to support clinical trials and research initiatives.
  • Leading the development and implementation of data analysis and reporting tools.
  • Collaborating with cross-functional teams to identify and prioritize statistical programming needs.
  • Designing and implementing data quality control and validation processes.
  • Developing and maintaining documentation and training materials for statistical programming tools and procedures.
  • Providing statistical programming support and guidance to junior team members.
Requirements

The following are some of the key requirements for this role:

  • Bachelor or Master’s degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field.
  • At least 5-6 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
  • Understanding of clinical data and drug development process, CDISC standards required.
  • Statistical Programming and SAS hand-on experience.
  • Clinical trials expertise with an understanding of data operations required for the reporting of clinical.
  • Good understanding of ICH and regulatory guidelines.
  • Working knowledge of clinical data and relevant data standards.
  • Ability to work with stakeholders across timezones under tight timelines.
  • Strong written and oral communication skills, and time and project management skills.
  • Strong competencies and interests for innovation and problem solving.
  • Proven ability to operate with limited oversight.
  • Knowledge of at least 1 Therapeutic Area.
What We Offer

We offer a competitive salary and benefits package, as well as opportunities for professional growth and development. If you are a motivated and talented Statistical Data Scientist who is passionate about delivering high-quality results, we encourage you to apply for this exciting opportunity.



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