Senior Associate, Database Analyst II, Clinical Database...

Role Summary

As part of the Data Monitoring and Management (DMM) group, an integral delivery unit within the Global Biometrics and Data Management (GBDM) organization, the Database Analyst II is responsible for the programming of high-quality clinical database and for the provision of expertise in clinical database technology. Responsible for supporting assigned segments of the Pfizer portfolio. Accountabilities to include the design, development, and maintenance of clinical databases ensuring the integrity of clinical data, application of standards supporting consistency in asset/submission data. The Clinical Database Analyst II learns how to mentor junior staff in database technologies and Pfizer standard database conventions. May serve as a subject matter expert on the design of ECRFs and clinical databases in one therapy area.

Role Responsibilities
• Works closely with department roles and cross-functional study team members to create data capture solutions that support the quality and timely delivery of data required per standard and study specific data review plans
• Complies with applicable SOPs and work practices
• Develops expertise in one or more technologies
• Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data

Basic Qualifications
• Bachelor's degree in a Life Science, Computer Science or equivalent
• Minimum of 2 years 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 and database programming skills
• Technical skills and experience using relational databases (e.g. Oracle InForm, Oracle DMW, MS SQL Server or MS Access)
• Strong communication (written and oral), decision-making, influencing, negotiation, and project management skills

Preferred Qualifications
• Proficiency in the use of Microsoft Office Suite of tools (Outlook, Word, Excel, etc.)
• Understanding of drug development process and data operations required for the reporting of clinical trial data (e.g. data review, study reports, regulatory submissions, safety updates, etc.)
• Understanding of regulatory requirements and relevant data standards; CDISC knowledge and experience are preferable

Pfizer is an equal opportunity employer and complies with all applicable equal employment opportunity legislation in each jurisdiction in which it operates.

Medical