Principal Statistical Data Scientist

Senior Associate, Principal Statistical Data Scientist

• An Individual Contributor role

• Productive hands on programming, supporting deliverables in the study/project/portfolio/standards team, of medium – high complex statistical programming deliverables to support assets and study teams

• Performs tasks independently with mentorship or advise from Programming Leads within the organization

• Acts as co-lead/lead on selected projects/initiatives/activities and also study deliverables as needed.

• Guide, mentor, monitor programmers within the team and collaborate with SDSL's on timelines, resource management and deliverables with quality.

• Is capable of handling standards/study programming specific activities independently including collaboration across stakeholders at various timezones

• Ensures adherence to high quality programming standards in their daily work

• Ensure the tasks are completed on time with quality and are compliant to the process at Pfizer with needed 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 to SDSA initiatives globally and locally.

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

• Accountable for their assigned work supporting the standards/study deliverables and also to assist SDSL's with the team assignments.

• Review/Develop/Validate/Review datasets, TFL as per CDISC aligned Pfizer Standards or Pfizer Data Standards for Study/Project/Portfolio. (Portfolio)

• Contributes to upto 80% of their time to programming deliverables assigned within the scope of the function in either SAS, R or Python and 20% to self learning, development and growth.

• Explore the existing code base and execute/perform runs as required, also develop/modify as per the needs and specifications suggested to the standards team as appropriate – (Standards Programming)

• Ensures appropriate documentation and QC across the lifespan of the study for all of their programming deliverables across Standards, Programming and Submissions.

• Understand/Implement standard/study/project/portfolio requirements and 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 complex problem solving skills, seeking direction when appropriate.

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

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

• Acts as mentor to junior team members

• Advances job knowledge to next level by participating/contributing in/to opportunities both globally and locally.

QUALIFICATIONS / SKILLS

• Bachelor or Master (preferred) Degree in Statistics, Computer Sciences, Engineering, Pharmacy, biological sciences, IT, or related field.

• At least 5 - 6 years 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

• Is able 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

Work Location Assignment: Flexible

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.