Database Analysts (Associate)--Clinical Data Collection Strategies
Pfizer
September 03, 2026
Remote friendly (Pearl River, NY)
United States
Clinical Research and Development
Role Responsibilities
- Work closely with department roles and cross-functional study team members to create data capture solutions that support quality and timely delivery of data 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 that support 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 pharmaceutical, biotech, CRO, or Regulatory Agency emphasizing building data collection and assimilation solutions
- Experience in Oracle, PL/SQL, SAS, Java, and relational database design
- Database programming skills
- Strong written, verbal, and presentation communication skills
- Proficiency in 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.
Benefits/Compensation (as stated)
- Base salary range: $68,600.00–$114,300.00
- Eligible for Global Performance Plan bonus target: 7.5%
- 401(k) with Pfizer matching contributions; additional retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/prescription/dental/vision.
- Work closely with department roles and cross-functional study team members to create data capture solutions that support quality and timely delivery of data 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 that support 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 pharmaceutical, biotech, CRO, or Regulatory Agency emphasizing building data collection and assimilation solutions
- Experience in Oracle, PL/SQL, SAS, Java, and relational database design
- Database programming skills
- Strong written, verbal, and presentation communication skills
- Proficiency in 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.
Benefits/Compensation (as stated)
- Base salary range: $68,600.00–$114,300.00
- Eligible for Global Performance Plan bonus target: 7.5%
- 401(k) with Pfizer matching contributions; additional retirement contribution; paid vacation/holidays/personal days; caregiver/parental and medical leave; medical/prescription/dental/vision.