Clinical Data Engineer: Study Database Design

Pfizer; Groton (CT); On-site; USD 68,000 - 114,000; Full time

Benefits offered by this job

401(k) with Pfizer Matching Contrib.

Comprehensive benefits package

Paid vacation/security leave

Job summary

Pfizer seeks a Clinical Database Programmer to design, develop, and maintain high-quality clinical databases supporting Pfizer's portfolio. You will ensure data integrity and apply data standards for asset/submission data.

You will collaborate with cross-functional study teams to deliver timely data capture solutions, comply with SOPs, and learn Pfizer database technologies, contributing to regulatory submissions and overall data quality.

Qualifications

• Bachelor’s degree in a Life Science discipline, Computer Science or other relevant discipline.
• Minimum of 1 year of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
• Experience in Oracle, PL/SQL, SAS, Java, relational database design
• Database programming skills
• Strong communication skills—written, verbal and presentation
• Proficiency in the use of Microsoft Office Suite of tools (e.g., Outlook, Word, Excel)

Responsibilities

• Program high-quality clinical databases and support assigned Pfizer portfolio.
• Design, develop, and maintain data capture solutions aligned with data standards.
• Collaborate with cross-functional study teams to deliver timely data.
• Ensure data integrity and compliance with SOPs and regulatory requirements.

Skills

Oracle

PL/SQL

SAS

Java

Relational database design

Database programming

Strong communication

Microsoft Office

Education

Bachelor’s degree in Life Science or Computer Science

Tools

Oracle InForm

Oracle DMW

MS SQL Server

MS Access

Job description

Pfizer seeks a Clinical Database Programmer to design, develop, and maintain high-quality clinical databases supporting Pfizer's portfolio. You will ensure data integrity and apply data standards for asset/submission data.

You will collaborate with cross-functional study teams to deliver timely data capture solutions, comply with SOPs, and learn Pfizer database technologies, contributing to regulatory submissions and overall data quality.