India - Chennai
Posted: Sep 02, 2026
On-siteFull-time
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Job Description

ROLE SUMMARY

As part of the Clinical Data Sciences (CDS) group, an integral delivery unit within the Clinical Development & Operations (CD&O) organization, the Associate Database Analyst is responsible for the programming of high-quality clinical databases. 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 Associate Database Analyst works with senior staff members to understand Pfizer standard database conventions and begins to understand the nuances of data collection needs between therapy 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

  • Develops expertise in one or more 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

  • Minimum 2 years of relevant experience in a pharmaceutical, biotech, CRO, or Regulatory Agency with an emphasis on building data collection and assimilation solutions

  • 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 learn more about acceptable and prohibited uses of AI during the recruitment process, please review our candidate AI-use guidelines available on Pfizer Careers.

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Additional Info
Min. Experience
-
Job Location Type
On-site
Job Type
Full-time
Predicted Seniority Level
-
Job Duration
-
Language(s)
-
Est. Budget/Pay Rate
To be discussed
Est. hrs
-
Optimal Job Start
-
Job Industry
-
Job Function
-
Employer
Pfizer
Preferred Applicant Countries
Global
Job Ref
J26A42A1361A5
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