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
• Learns Pfizer database 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
• Any years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions will be considered as a plus
• Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills

PREFERRED QUALIFICATIONS

• 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
• 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

Work Location Assignment: Hybrid

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

To apply please visit our website www.pfizercareers.com and search job Associate Database Programmer Analyst, Clinical Database Management id 4938609.

Please apply by sending your CV in English.