at Pfizer
Full Time•Accountable for the quality and timely deliveryof 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.
•At least 5+ years relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency.
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
