Database Analyst II, Clinical Database Management

Database Analyst II, Clinical Database Management

Pfizer Asia Pacific Pte Ltd
Beijing China
5-8 years
Not Specified

Job Description


Job Description :
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 Senior Database Analyst 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 Senior Database Analyst mentors junior staff in database technologies and Pfizer standard database conventions. Serves as a subject matter expert on the design of ECRFs and clinical databases across one or more therapeutic areas.
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
  • Serves as subject matter expert in one or more technologies
  • Leads and contributes to cross-functional technical initiatives in collaboration with Pfizer Business Technology and other teams

Supports knowledge development 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 5 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions
  • Technical skills and experience using relational databases (e.g. Oracle InForm, Oracle DMW, MS SQL Server or MS Access)
  • Experience in Oracle, PL/SQL, SAS, Java, relational database design and database programming skills
  • 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

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Pfizer careers are like no other. In our culture of individual ownership, we believe in our ability to improve future healthcare, and potential to transform millions of lives. We’re looking for new talent to join our global community, to unearth new innovative therapies that make the world a healthier place.

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