Pfizer Hiring Data Specialist: In 2024, Pfizer, a reputable firm, will have an Off Campus Drive whereby it will provide openings for entry-level positions like Junior Lab Data Specialist Office. A bachelor’s degree in any subject is acceptable for application to the Pfizer off-campus drive in 2024. Candidates who meet the requirements can review further information below.
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About Pfizer
Careers at Pfizer are unlike any other. We think we have the power to change millions of lives and advance healthcare in the future in our culture of individual ownership. We are seeking fresh talent to become a part of our worldwide community and discover novel, cutting-edge treatments that improve health throughout the globe.
Pfizer Hiring Data Specialist Details
Job Role: Data Specialist
Company Website: www.pfizer.com
Qualification: Graduate
Experience: Freshers/Experienced
Batch: Recent Batches
Salary: As per company standards
Location: Chennai
Last Date: ASAP
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Roles & Responsibilities
Below are the Roles & Responsibilities –
- To develop new lab (identifiers) IDs in EDC systems, review lab slips and papers for Normal Reference Ranges for all protocol-required lab tests.
- Maintenance of Lab IDs and changes within standard database reference ranges.
- Support all Pfizer study lab IDs, including central and local.
- Textbook Reference Points updates and requests.
- Help with the assignment of lab codes to tests for incoming lab data via electronic transfer or the CRF.
- Respect all SOP documentation and rules pertaining to the lab.
- Gives the research administration direction on how to get correct and comprehensive Reference range papers from Investigator locations.
- Gives the study team direction for assigning Lab IDs, analyzing all study lab data, and resolving assignment problems.
- Assist data managers in reviewing and perhaps resolving conflicts in lab data related to research conduct and reporting.
- Use the Pfizer browser tools and programs to run Lab Data listings and reports.
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Required Skills & Qualifications
Below are the Required Skills & Qualifications –
- A life science bachelor’s degree and between one and one and a half to one year of relevant work experience in a biotech, pharmaceutical, CRO, or regulator agency, with a focus on safety lab data solutions.
- Clinical trial data reporting requires an understanding of the drug development process and data operations (e.g., data review, study reports, regulatory filings, safety updates, etc.).
- It is preferred to have CDISC training and expertise.
- Excellent decision-making, persuasion, negotiation, writing and spoken communication, and project management abilities
- Knowledge of EDC systems including Oracle Clinical, Data Labs, Rave, and InForm as well as clinical data management.
- A solid grasp of the procedures involved in gathering data from laboratory tests (including the units acollected)
- Proficiency with the Microsoft Office suite of programs, including Word, Excel, and Outlook.
- Understanding and/or familiarity with relational databases (like Oracle) and tools for data visualization and reporting (like J Review and Spotfire).
- Experience working in clinical diagnostic labs or hospitals.
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