Clinical Data Analyst (Associate)
Pfizer is seeking a Database Analyst (Associate) to join the Clinical Data and Information Sciences (CDIS) group within our Research & Development organization. This role is ideal for candidates with a strong technical background who are passionate about data integrity and clinical research. You’ll play a key role in designing, building, and maintaining clinical databases that support high-quality, timely data collection and reporting across global studies. Working closely with cross-functional teams, you’ll help ensure Pfizer’s clinical data systems meet internal standards and regulatory expectations. This is a fantastic opportunity to grow your skills in a meaningful area of healthcare, while supporting breakthrough medicines that change lives. If you're experienced in relational databases, have programming skills, and want to work in a mission-driven organization, we encourage you to apply
Application is received untill position is filled
Requirements
1. Bachelor’s degree in Life Sciences, Computer Science, or related field
2. Minimum 1 year of technical experience in pharma, biotech, CRO, or regulatory setting
3. Strong programming skills (Oracle, PL/SQL, SAS, or Java)
4. Experience with relational databases (e.g., Oracle InForm, DMW, SQL Server)
5. Excellent verbal and written communication skills
6. Familiarity with regulatory standards and CDISC is a plus
7. Must be authorized to work in the U.S.
Benefits
1. Competitive base salary
2. Performance bonus
3. Comprehensive health benefits (medical, dental, vision)
4. 401(k) with Pfizer match and retirement savings contributions
5. Paid vacation, holidays, and caregiver/parental leave
6. Relocation assistance (based on eligibility)
7. Opportunities to work on global clinical trials
8. Access to continuous training and professional development
Responsibilities
1. Design, develop, and maintain high-quality clinical databases
2. Ensure database structures support data consistency and integrity
3. Implement data capture solutions aligned with clinical study needs
4. Collaborate with study teams and cross-functional departments
5. Apply relevant standards and SOPs in daily work
6. Monitor and troubleshoot data systems to ensure accuracy
7. Assist in preparing datasets for regulatory submissions
8. Support data quality through testing and process improvements
The application process will continue on the employer's website.
Location
Pearl River, NY New York City, NY Groton, CT Collegeville, PA, United States