Senior Associate, Senior Statistical Data Scientist

Senior Associate, Senior Statistical Data Scientist

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

To fully realize Pfizer’s purpose – Breakthroughs that change patients’ lives – we have established a clear set of expectations regarding “what” we need to achieve for patients and “how” we will go about achieving those goals.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

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.

Role 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.

Experience & Skills:

Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.

At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency

Strong written and oral communication skills, and project management skills

Proven ability to operate with limited oversight

Proven ability to manage delivery under tight timelines.

Statistical Programming and SAS/R/Python hands-on experience

Preferrable but optional:

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

Knowledge of at least 1 Therapeutic Area

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

Work Type: Hybrid

#LI-PFE

Work Location Assignment:Flexible

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.

Role 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.

Experience & Skills:

• Bachelor or Master (preferred) Degree in Statistics, Biological Sciences, IT, or related field.
• At least 3 years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency
• Strong written and oral communication skills, and project management skills
• Proven ability to operate with limited oversight
• Proven ability to manage delivery under tight timelines.
• Statistical Programming and SAS/R/Python hands-on experience

Preferrable but optional:

• 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
• Knowledge of at least 1 Therapeutic Area
• 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.

Work Type: Hybrid

#LI-PFE

Work Location Assignment:Flexible

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