Database Analysts (Associate)--Clinical Data Collection Strategies
Pfizer
September 03, 2026
Remote friendly (New York, NY)
United States
IT
Role Summary
- Program high-quality clinical databases to support assigned segments of the Pfizer portfolio.
- Design, develop, and maintain clinical databases to ensure data integrity and consistent asset/submission data standards.
Role Responsibilities
- Work with department and cross-functional study team members to create data capture solutions supporting quality and timely delivery per standard and study-specific data review plans.
- Comply with applicable SOPs and work practices.
- Learn Pfizer database technologies.
- Develop knowledge of data capture tools and methods supporting accuracy and integrity of study data.
Minimum Qualifications
- Bachelor’s degree in a Life Science discipline, Computer Science, or other relevant discipline.
- 1+ year of relevant experience in pharma/biotech/CRO/Regulatory Agency emphasizing data collection and assimilation solutions.
- Experience with Oracle, PL/SQL, SAS, Java, and relational database design.
- Database programming skills.
- Strong written, verbal, and presentation communication.
- Proficiency with Microsoft Office Suite (Outlook, Word, Excel).
Preferred Qualifications
- Experience with relational databases (e.g., Oracle InForm, Oracle DMW, MS SQL Server, MS Access).
- Understanding of drug development process and clinical trial data operations (data review, study reports, regulatory submissions, safety updates).
- Understanding of regulatory requirements and relevant data standards.
Work Location
- On-site average 2.5 days/week; live within commuting distance.
Compensation/Benefits
- Base salary range: $68,600–$114,300; eligible for Global Performance Plan bonus target of 7.5%.
- Benefits include 401(k) with matching, paid vacation/holidays/personal days, caregiver/parental and medical leave, and medical/prescription/dental/vision coverage.
- Program high-quality clinical databases to support assigned segments of the Pfizer portfolio.
- Design, develop, and maintain clinical databases to ensure data integrity and consistent asset/submission data standards.
Role Responsibilities
- Work with department and cross-functional study team members to create data capture solutions supporting quality and timely delivery per standard and study-specific data review plans.
- Comply with applicable SOPs and work practices.
- Learn Pfizer database technologies.
- Develop knowledge of data capture tools and methods supporting accuracy and integrity of study data.
Minimum Qualifications
- Bachelor’s degree in a Life Science discipline, Computer Science, or other relevant discipline.
- 1+ year of relevant experience in pharma/biotech/CRO/Regulatory Agency emphasizing data collection and assimilation solutions.
- Experience with Oracle, PL/SQL, SAS, Java, and relational database design.
- Database programming skills.
- Strong written, verbal, and presentation communication.
- Proficiency with Microsoft Office Suite (Outlook, Word, Excel).
Preferred Qualifications
- Experience with relational databases (e.g., Oracle InForm, Oracle DMW, MS SQL Server, MS Access).
- Understanding of drug development process and clinical trial data operations (data review, study reports, regulatory submissions, safety updates).
- Understanding of regulatory requirements and relevant data standards.
Work Location
- On-site average 2.5 days/week; live within commuting distance.
Compensation/Benefits
- Base salary range: $68,600–$114,300; eligible for Global Performance Plan bonus target of 7.5%.
- Benefits include 401(k) with matching, paid vacation/holidays/personal days, caregiver/parental and medical leave, and medical/prescription/dental/vision coverage.