Database Analysts (Associate)--Clinical Data Collection Strategies

Role: Clinical Data Programmer responsible for designing, developing, and maintaining high-quality clinical databases to support Pfizer's clinical trial data management. Objectives include ensuring data integrity, applying standards for asset and submission consistency, and supporting data review processes. Responsibilities encompass collaborating with cross-functional teams to develop data capture solutions, ensuring compliance with SOPs, and gaining proficiency in Pfizer's database technologies, including relational database tools. Qualifications: Bachelor's in Life Sciences, Computer Science, or relevant fields; at least 1 year of experience in data solutions within pharma, biotech, CRO, or regulatory agencies; proficiency in Oracle, PL/SQL, SAS, Java, and database programming; strong communication skills. Preferred: experience with relational databases like Oracle InForm or MS SQL Server, understanding of clinical data operations for trial reporting, and familiarity with regulatory data standards. High-Value: Focus on clinical data management in a pharma setting, supporting clinical trial phase data collection and submission processes, with an onsite requirement averaging 2.5 days/week at the location specified. Travel and remote work details are not specified.