Join Pfizer as a Junior Central Testing Analyst – Explore a Career in Cutting-Edge Pharmaceutical Innovation

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Welcome to an exciting career opportunity at one of the world’s leading pharmaceutical innovators! Pfizer, a global healthcare company, is pleased to announce a vacancy for the position of Junior Central Testing Analyst. If you are a driven and detail-oriented professional looking to make a meaningful impact in the pharmaceutical industry, this role provides a unique chance to contribute to cutting-edge research and development.

Junior Central Testing Analyst

As a Junior Central Testing Analyst at Pfizer, you’ll be part of a dynamic team committed to advancing healthcare through innovation and excellence. This position offers a gateway to the heart of pharmaceutical research, allowing you to play a key role in the analysis and testing processes that underpin Pfizer’s commitment to quality and efficacy.

Job Description
Role Summary
As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Pfizer Research and Development (PRD) organization, the Junior Central Testing Analyst is responsible for performing User Acceptance Testing of database screens in accordance with protocol and ensure the end users can enter the data as per the standards and expectation. In addition to the screen testing the Junior Central Testing Analyst will also be responsible to perform the testing of edit check to ensure the checks are rightly programmed, appropriate and adequate as per the specification.

Role Responsibilities
• Perform activities, including but not limited to the testing of CRF design, Acquisition & Processing of electronic data, such as external eData, Lab Data and PK/PD Data, database edit checks under appropriate oversight.
• Accountable for high quality and on time delivery for assigned deliverables.
• Ensure the consistent use and application of applicable data standard and ensures data quality and consistency across programs and repositories.
• Ensure work carried out in accordance with applicable SOPs and working practices.
• Understand the Protocol to perform Screen testing.
• Participate in UAT feedback meetings.
• Track the lessons learned and share the knowledge across the team.
• Complete all the documentation related to study and share it with study Team.

Candidate Profile
• Awareness of clinical development and pharmaceuticals as a regulated industry
• Awareness of healthcare regulatory authorities (e.g., FDA, Health Canada)
• Ability to learn clinical data management processes and principles in area of responsibility.
• Demonstrates required verbal and written communication skills including ability to communicate remotely.
• Capable to learn technical data systems.
• Capable to learn how to use data visualization tools (e.g. Spotfire, J-Review)
• Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
• Knowledge and experience in functional / automation testing, SDLC, database management role, understanding key processes and principles associated with role including CRF design, database set-up, edit check specification, data transfer activities preferred.
Primarily an office-based position involving sitting in front of a computer for large periods of work time, making presentations, etc.

Last Date: 20th December 2023

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