Database Analysts (Associate)--Clinical Data Collection Strategies

Role: Clinical Data Programmer supporting Pfizer's clinical trials by designing, developing, and maintaining high-quality databases to ensure data integrity and compliance with standards. Responsibilities include collaborating with cross-functional teams to create data capture solutions aligned with study review plans, adhering to SOPs, and learning Pfizer's database technologies. Qualifications: Bachelor's in Life Sciences, Computer Science, or related field; at least 1 year of experience in data solutions within pharma, biotech, CRO, or regulatory agencies; proficiency in Oracle, PL/SQL, SAS, Java, and relational databases; strong communication skills. Preferred: experience with relational databases like Oracle InForm or MS SQL Server; understanding of drug development data operations, regulatory standards, and clinical trial reporting. Work: On-site (average 2.5 days/week), in the U.S., with potential relocation assistance. This role emphasizes data management expertise in clinical development processes, particularly for Pfizer's ongoing trials.