• 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.
Work Location Assignment: Flexible
Work Location Assignment: Flexible
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.
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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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Employees engage in a combination of remote and on-site work.
