Manager, Statistical Data Sciences Lead (IC)

Posted Yesterday
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Makati City, Metro Manila, National Capital Region, PHL
In-Office
Senior level
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 programmer delivering analysis-ready datasets, tables, listings, and figures for clinical studies. Acts as study-level programming point of contact, ensures quality standards and regulatory compliance, supports asset/submission activities, manages/mentors remote global team members, and communicates technical results to non-technical stakeholders using SAS, R, and Python.
Summary Generated by Built In
Role Summary
  • A highly productive, independent programming lead ensuring excellence in the delivery of analysis ready datasets, tables, listings, and figures to advance research, development, and commercialization of the Pfizer portfolio following Pfizer SOPs and processes
  • This role is the programming point of contact at the study level, and will support at the asset/submission level.
  • Ensures adherence to high quality programming standards in the production of clinical reports.

Qualifications
  • Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
  • At least 5 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
  • Statistical Programming and SAS/R/Python hands-on experience
  • Routine problem-solving skills, developing the ability to solve complex problems using skills based on experience and extrapolation to new situations.
  • Extensive knowledge of routine statistical methodology and its application to programming
  • Knowledge of vendor processes
  • Demonstrated experience in developing successful partnerships within study teams
  • Strong written and oral communication skills, and project management skills
  • Ability to present technical information to a non-technical audience
  • Proven ability to operate independently.
  • Some exposure working across international boundaries and cultures.
  • Ability to manage customer expectations.
  • Ability to manage work of others in a remote and/or global setting

Preferred, but not Required
  • Clinical trials expertise with a thorough understanding of data operations required for the reporting of clinical trial data.
  • Thorough understanding of clinical data and relevant data standards
  • Good understanding of ICH and Regulatory Guidelines
  • CDISC experience highly desirable.

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
Medical
#LI-PFE
Work Location Assignment: Hybrid
Work Location Assignment: Hybrid
Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.
To learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers .
Medical

Skills Required

  • Bachelor's degree in Statistics, Biological Sciences, IT, or related field
  • Master's degree
  • At least 5 years relevant experience in pharmaceutical, biotech, CRO, or Regulatory Agency
  • Hands-on statistical programming experience
  • Hands-on experience with SAS
  • Hands-on experience with R
  • Hands-on experience with Python
  • Extensive knowledge of routine statistical methodology and its application to programming
  • Routine problem-solving skills for complex situations
  • Knowledge of vendor processes
  • Demonstrated experience developing partnerships within study teams
  • Strong written and oral communication skills
  • Project management skills
  • Ability to present technical information to non-technical audiences
  • Proven ability to operate independently
  • Some exposure working across international boundaries and cultures
  • Ability to manage customer expectations
  • Ability to manage work of others in a remote and/or global setting
  • Clinical trials expertise (preferred)
  • Thorough understanding of clinical data and relevant data standards (preferred)
  • Good understanding of ICH and regulatory guidelines (preferred)
  • CDISC experience (highly desirable)

What the Team is Saying

Daniel
Anna
Esteban
Pfizer

Pfizer Compensation & Benefits Highlights

  • Healthcare Strength Multiple U.S. medical plan options include telehealth, comprehensive mental‑health support, fertility/family‑building benefits, transgender‑inclusive coverage, and certain Pfizer medications at no cost. A Wellbeing Wallet and wellness resources broaden the health and wellbeing offering.
  • Retirement Support A 401(k) with company matching is paired with an additional Pfizer Retirement Savings Contribution, alongside company‑paid life and disability insurance. One‑on‑one financial planning support is provided through Fidelity.
  • Leave & Time Off Breadth Paid time off spans vacation, holidays, and personal days, with additional caregiver and medical leave. U.S. parental leave commonly includes 12 weeks paid with options for additional unpaid bonding time and a return‑to‑work transition.

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The Company
HQ: New York, NY
121,990 Employees
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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Pfizer Offices

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Employees engage in a combination of remote and on-site work.

Typical time on-site: 2.5 days a week
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