Senior Associate, Senior Lab Data Specialist
Pfizer (company site, opens in a new tab)3–5 yrsChennaiOn-siteDirect career pageEst. 9–16 LPA
Posted 7h ago
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Job description
Structured overview of role & requirements
About This Role
- Own configuration and maintenance of Lab Normal Management Tool and lab identifiers in EDC systems for Pfizer studies.
- Serve as technical SME for lab data standards implementation, lab CRF design support, lab data discrepancy resolution, and creation/testing of lab data reports.
- Drive process improvements, develop SOPs/guidelines, and ensure operational excellence in safety lab data management and deliverables across studies.
Minimum Requirements
- BS degree in life sciences with 3-5 years relevant experience in pharmaceutical, biotech, CRO, or regulatory agency focusing on safety lab data solutions.
- Experience in clinical data management, EDC systems, and understanding of lab data collection and drug development data operations.
- Preferably knowledge of CDISC standards and experience with relational databases (e.g., Oracle) and data visualization tools (e.g., Spotfire, J Review).
- Work Location: On Premise; Ability to travel ~5%. Work Experience Required: 3-5 years; Other specific notice period not mentioned.
Ideal Candidate Profile
- Experienced in safety lab data operations within clinical trials with strong understanding of lab test units, reference ranges, and data standards implementation.
- Skilled in collaborating with cross-functional teams including data managers, clinical teams, and vendors to ensure data accuracy and integrity in large pharmaceutical studies.
- Capable of leading process improvements, SOP development, and supporting organizational initiatives related to lab data management and reporting.