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Medium — Tier-1 employer and metro location increase competition, while clinical specialization limits applicant pool.
High — clinical data standards and regulatory knowledge reduce transferability across industries.
High — explicit years, mandatory database/clinical tools, and regulated CDISC/regulatory requirements.
Design, develop, and maintain high-quality clinical databases ensuring data integrity for assigned Pfizer portfolio segments.
Collaborate with cross-functional study teams to create data capture solutions supporting quality and timely data delivery per study-specific review plans.
Apply standard database conventions and support consistency in clinical data collection aligned with regulatory standards.
Bachelor's degree in Life Science, Computer Science, or equivalent.
Minimum 2 years experience in pharmaceutical, biotech, CRO, or regulatory agency focused on data collection and assimilation solutions.
Experience with Oracle, PL/SQL, SAS, Java, relational database design, and programming.
Work Location: Hybrid.
Operational experience in clinical data management with exposure to drug development processes and clinical trial data operations.
Technical proficiency with relational databases and clinical data standards, preferably including CDISC knowledge.
Ability to engage with cross-functional teams and apply regulatory data standards for clinical submissions.