Associate, Associate Database Analyst

Chennai - India

Monthly Salary: Not Disclosed

Posted on: Yesterday

Vacancies: 1 Vacancy

Job Summary

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

Bachelors 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.

Medical

Required Experience:

ROLE SUMMARYAs 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 ...

ROLE SUMMARY

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

Bachelors 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.

Medical

Required Experience:

Key Skills

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About Company

Pfizer

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