Senior Associate, Database Analyst, Clinical Database Management

Pfizer, S.A. de C.V; Chennai District; Hybrid; INR 600,000 - 1,000,000; Full time

Job summary

Pfizer’s Clinical Data Sciences group seeks a Senior Associate, Database Analyst to design, develop, and maintain high-quality clinical databases. You will ensure data integrity and align with Pfizer standards across therapy areas while supporting portfolio segments.

In this role, you will work with senior staff to understand data collection needs and apply data capture tools and methods. The position emphasizes collaboration, regulatory awareness, and continuous learning in a hybrid work

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.

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.

Skills

Oracle

PL/SQL

SAS

Java

Relational database design

Database programming

Education

Bachelor's degree in Life Science, Computer Science or equivalent

Job description

Senior Associate, Database Analyst, Clinical Database Management

We’re in relentless pursuit of breakthroughs that change patients’ lives. We innovate every day to make the world a healthier place.

Pfizer Research & Development serves as the beating heart of Pfizer's trailblazing product pipeline, the essence of our mission to bring life-changing medicines to the world.

Pfizer offers competitive compensation and benefits programs designed to meet the diverse needs of our colleagues.

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

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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