Statistical Data Sciences Lead

Posted 7 Days Ago
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Chennai, Tamil Nadu
Hybrid
5-7 Years Experience
Artificial Intelligence • Healthtech • Machine Learning • Natural Language Processing • Biotech • Pharmaceutical
We’re in relentless pursuit of breakthroughs that change patients’ lives.
The Role
Lead statistical data scientist responsible for delivering statistical programming deliverables to support assets and study teams. Ensures high-quality programming standards and timely delivery of datasets for clinical study reports. Requires Bachelor's or Master's degree in Statistics, 8-15 years of experience in pharmaceutical or biotech industry, statistical programming and SAS experience, clinical trials expertise, knowledge of ICH and regulatory guidelines, and strong communication and project management skills.
Summary Generated by Built In
  • JOB SUMMARY
    • A productive, hands-on programmer who applies technical knowledge and practical experience to deliver statistical programming deliverables to support assets and study teams with limited supervision early in role and independently later in role.
    • Ensures excellence in the programming of analysis ready datasets, tables, listings, and figures for which they are responsible
    • Ensures adherence to high quality programming standards in their daily work.
    JOB RESPONSIBILITIES
    • Accountable for the quality and timely delivery of datasets and displays required for their clinical study reports as well as other asset level deliverables they may be programming
    • Ensures appropriate documentation and QC across the lifespan of the study for all of their Programming deliverables
    • Exhibits routine and occasionally complex problem solving skills, seeking direction when appropriate.
    • Works with statisticians and programming leads to ensure clear specifications for their programmed deliverables are in place.
    • Will be knowledgeable in core safety standards as well as TA standards pertinent to their project, may aid in development of standards necessary for their study may contribute to department level initiatives.
    QUALIFICATIONS / SKILLS
    • Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
    • At least 8-15 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
    • Statistical Programming and SAS hand-on experience
    • Clinical trials expertise with an understanding of data operations required for the reporting of clinical trial data.
    • Good understanding of ICH and regulatory guidelines
    • Working knowledge of clinical data and relevant data standards
    • Strong written and oral communication skills, and project management skills
    • Proven ability to operate with limited oversight
    • Knowledge of at least 1 Therapeutic Area
    • Proven ability to manage delivery under tight timelines.
    • CDISC experience desirable


Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical

Top Skills

SAS

What the Team is Saying

Daniel
Anna
Esteban
The Company
HQ: New York, NY
121,990 Employees
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Year Founded: 1848

What We Do

Our purpose ensures that patients remain at the center of all we do. We live our purpose by sourcing the best science in the world; partnering with others in the healthcare system to improve access to our medicines; using digital technologies to enhance our drug discovery and development, as well as patient outcomes; and leading the conversation to advocate for pro-innovation/pro-patient policies.

Why Work With Us

We are the inventors, the problem solvers, the big thinkers — those who surmount any hurdle to deliver breakthrough medicines to the people who are counting on them the most.

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