Hybrid Life Science Job at Pfizer
Looking for a dynamic Life Science Job in a global pharmaceutical leader? Pfizer Careers is offering an exciting hybrid job opportunity for the role of Associate Database Analyst in Chennai. This is a perfect opportunity for life science graduates who want to work in clinical data sciences and contribute to impactful drug development projects.
About Pfizer
Pfizer Inc., one of the world’s leading biopharmaceutical companies. With a strong focus on innovation and patient care, Pfizer delivers breakthrough medicines globally. It offers excellent Life Science Jobs, including Hybrid Job roles, creating a strong opportunity for life science graduates to build impactful careers.
Job Details:
- Job Title: Associate / Associate Database Analyst
- Company: Pfizer
- Location: Chennai, India
- Job Type: Full-Time | Hybrid
Role Summary
The Associate Database Analyst is part of the Clinical Data Sciences (CDS) group, a key delivery unit within Clinical Development & Operations (CD&O). The role focuses on programming and maintaining high-quality clinical databases to support segments of the Pfizer portfolio.
The position involves designing, developing, and maintaining clinical databases while ensuring data integrity and adherence to standardized processes. The analyst collaborates with senior team members to understand database standards and data collection requirements across different therapeutic areas.
Roles & Responsibilities
- Collaborates with cross-functional study teams to develop data capture solutions that ensure timely and high-quality data delivery.
- Supports study-specific data review plans while maintaining consistency with organizational standards.
- Ensures compliance with applicable Standard Operating Procedures (SOPs) and work practices.
- Designs, develops, and maintains clinical databases to support clinical trial activities.
- Applies data standards to ensure consistency across assets and regulatory submissions.
- Develops expertise in relevant technologies and tools used in clinical data management.
- Enhances understanding of data capture methods to improve data accuracy and integrity.
Basic Qualifications
- Bachelor’s degree in Life Sciences, or a related field.
- Minimum of 2 years of relevant experience in pharmaceutical, biotechnology, CRO, or regulatory environments.
- Experience in building data collection and data integration solutions.
- Proficiency in Oracle, PL/SQL, SAS, Java, and relational database design/programming.
Preferred Qualifications
- Experience with relational database tools such as Oracle InForm, Oracle DMW, MS SQL Server, or MS Access.
- Strong communication, decision-making, negotiation, and project management skills.
- Proficiency in Microsoft Office tools (Outlook, Word, Excel).
- Understanding of the drug development lifecycle and clinical data operations, including:
- Data review processes
- Study reporting
- Regulatory submissions
- Safety data updates
- Familiarity with regulatory requirements and clinical data standards, including CDISC (preferred).
Work Location
Hybrid work model based in Chennai, India.
