• An Individual Contributor role

  
  
  

• Productivehands onprogramming, supporting deliverables in the study/project/portfolio/standards team, ofmedium – highcomplex statistical programming deliverablesto support assets and study teams 

  
  
  

• Performs tasksindependentlywith mentorship or advise from Programming Leads within the organization 

  
  
  

• Acts as co-lead/lead on selected projects/initiatives/activitiesand alsostudy deliverables as needed.

  
  
  

• Guide, mentor, monitor programmers within the team and collaborate with SDSL’s on timelines, resourcemanagement  anddeliverables with quality. 

  
  
  

• Is capable of handling standards/study programming specific activities independently including collaboration acrossstakeholders at varioustimezones

  
  
  

• Ensures adherence tohigh qualityprogramming standards in their daily work

  
  
  

• Ensure the tasks are completed on time with quality and are compliant to the processat  withneeded guidance. 

  
  
  

• Work collaboratively with study teams and stakeholders such as clinicians and statisticians on milestones and deliverables.

  
  
  

• Active self-learning and delivering on solutions in the space of statistical programming and data standards 

  
  
  

• Contribute toSDSAinitiatives globally and locally. 

  
  
  

Job Responsibilities

• Accountable formultiple projects/ongoing work activities (timelines, work plans, deliverables) of moderate complexity within a Work Team

  
  
  

• Accountable for their assigned work supporting the standards/study deliverablesand alsotoassistSDSL’s with the team assignments. 

  
  
  

• Review/Develop/Validate/Reviewdatasets, TFL as per CDISCaligned  Standardsor  DataStandards for Study/Project/Portfolio. (Portfolio)

  
  
  

• Contributestoupto80% of their time toprogramming deliverables assigned within the scope of the function in either SAS, R or Pythonand 20% toself learning,developmentand growth. 

  
  
  

• Explore the existing code base and execute/perform runs asrequired, also develop/modifyas per the needs and specifications suggested to the standards team asappropriate –(Standards Programming)

  
  
  

• Ensures appropriate documentation and QC across the lifespan of the study forall oftheirprogramming deliverablesacross Standards, Programming and Submissions.

  
  
  

• Understand/Implementstandard/study/project/portfolio requirementsand specification and work with global stakeholders in ensuring completion of project/study/deliverable goals and milestones

  
  
  

• Knowledgeable in core safety standards as well as TA standards pertinent to their project and lead development of standards necessary for their study

  
  
  

• Exhibits routine and occasionally complexproblem solvingskills, seeking direction whenappropriate.

  
  
  

• Regularly update leads on progress and time estimations to ensure smooth daily operations andaccurateplanning

  
  
  

• Support in accomplishing department and organization mission by completing assigned tasks

  
  
  

• Acts as mentor to junior team members

  
  
  

• Advances job knowledge tonextlevel byparticipating/contributing in/to opportunities both globally and locally.

  
  
  

Basic Qualifications:

• Bachelor or Master (preferred) Degree in Statistics,Computer Sciences, Engineering,Pharmacy, biologicalsciences, IT, or relatedfield.

  
  
  

• At least5 - 6years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.

  
  
  

• Understandingof clinical data and drug development process, CDISC standardsrequired

  
  
  

• Statistical Programming and SAS hand-on experience

  
  
  

• Clinical trialsexpertisewith 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

  
  
  

• Is able towork with stakeholders acrosstimezonesunder tight timelines

  
  
  

• Strong written and oral communication skills, and timeand projectmanagement skills

  
  
  

• Strong competencies and interests for innovation and problem solving

  
  
  

• Proven ability tooperatewith limited oversight

  
  
  

• 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.