Database Analyst (associate)--clinical Data Collection Strategies

Pfizer Pfizer · Pharma · Buenos Aires, Latin America, Argentina

This role is responsible for the programming of high-quality clinical databases, supporting assigned segments of the Pfizer portfolio. Accountabilities include the design, development, and maintenance of clinical databases, ensuring data integrity and applying standards for consistency in asset/submission data. It involves close collaboration with study team members to create data capture solutions and ensuring compliance with SOPs and work practices.

What you'd actually do

  1. 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
  2. Complies with applicable SOPs and work practices
  3. Learns Pfizer database technologies
  4. Develops knowledge of data capture tools and methods that support the accuracy and integrity of study data

Skills

Required

  • Bachelor's degree in a Life Science, Computer Science or equivalent
  • Minimum of 1 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency
  • Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills

Nice to have

  • 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

What the JD emphasized

  • Minimum of 1 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions