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Tier-1 brand, popular mid-level project role, and metro location increase applicant competition.
Clinical trial database skills and regulatory compliance needs limit cross-industry transferability.
Requires clinical database subject-matter expertise and compliance knowledge despite lacking explicit years, so moderate filtering.
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Lead project management for clinical database design, development, and maintenance within Clinical Data Sciences for assigned Pfizer portfolio segments.
Ensure integrity, consistency, and compliance of clinical data through oversight of database build lifecycle and change control, applying Pfizer standards.
Serve as Subject Matter Expert in database build for assigned Therapy Area and collaborate closely with Clinical Data Scientists to deliver consistent, timely, and high-quality clinical database solutions.
Experience with clinical database management and project management in clinical data sciences or related field: Not explicitly quantified in JD but indicated by role seniority and responsibilities.
Strong knowledge of clinical database build lifecycle, change control processes, and Pfizer standards compliance.
Ability to solve moderately complex problems in database build and implementation and perform impact analysis communicating with technical and non-technical stakeholders.
Work Location Assignment: Hybrid. Notice period and mandatory degrees or certifications: Not explicitly mentioned in the JD.
Experienced in managing cross-functional study teams and leading internal initiatives to improve clinical data capture processes within pharmaceutical or clinical research settings.
Demonstrated expertise as a Subject Matter Expert in clinical database build, capable of ensuring operational excellence and collaboration across data management and clinical data science functions.
Capable of independently assessing impact of changes, developing mitigation plans, and driving innovative process/product improvements beyond immediate discipline boundaries.