Associate, Associate Database Analyst, Clinical Database Management

Pfizer; Chennai District; Hybrid; INR 600,000 - 900,000; Full time

Job summary

Pfizer, a global leader in healthcare, seeks a Data Monitoring and Management professional to ensure the accuracy and integrity of clinical trial data in a hybrid Chennai-based role. You will perform DMM activities, data reviews, query handling, and support CTMS inquiries from study teams.

The role requires a BA/BS, ICH/GCP experience, familiarity with EDC/EDC tools, and strong English communication. Collaboration with TMF owners and document teams will be essential.

Qualifications

• BA/BS degree in a life sciences or equivalent.
• Hands-on experience with ICH/GCP documentation requirements.
• Familiarity with electronic data capture and documentation management systems.
• Understanding of clinical development processes and data standards.
• Strong English communication skills.
• Proficiency in Microsoft Office.

Responsibilities

• Engage in Data Monitoring and Management (DMM) activities, including data review and query management.
• Ensure the quality of database design through documentation, testing, validation, and implementation of clinical data collection tools.
• Serve as the first point of contact for CTMS questions and issues.
• Adhere to SOPs and working practices.
• Collaborate with Study Team Points of Contact, Document Owners, and TMF Study Owners to resolve discrepancies.
• Contribute to process improvement initiatives and projects.

Skills

Clinical Data Management

Documentation management

ICH/GCP knowledge

MS Office

Education

BA/BS degree

Tools

CTMS

EDC systems

Electronic documentation management systems

Job description

Use Your Power for Purpose At Pfizer, our Worldwide Medical and Safety colleagues are pivotal in bridging evidence-based medical decision support with stakeholders to enhance health and treatment outcomes. Whether you are developing frameworks to ensure our evidence is scientifically robust, offering unbiased and medically essential expertise, or exploring ways to address data gaps, our mission remains clear: to empower healthcare decisions regarding the safe and appropriate use of medicines for patients. You will play a crucial role in improving patients' lives by ensuring the accuracy and integrity of clinical data. Your work will directly impact the development of new treatments and therapies, helping to bring innovative solutions to patients in need.

What You Will Achieve

• Engage in Data Monitoring and Management (DMM) activities, including data review, query management, and investigating logic check flags.
• Ensure the quality of database design through documentation, testing, validation, and implementation of clinical data collection tools or systems.
• Serve as the first Point of Contact for customers needing assistance with Clinical Trial Management System (CTMS) questions and issues.
• Adhere to applicable Standard Operating Procedures (SOPs) and working practices.
• Collaborate with Study Team Points of Contact, Document Owners, and Trial Master File (TMF) Study Owners to resolve document-related discrepancies and issues.
• Contribute to process improvement initiatives and additional projects as they arise.

Here Is What You Need (Minimum Requirements)

• BA/BS with any years of experience
• Demonstrated experience of ICH/GCP (International Council for Harmonization/Good Clinical Practice) documentation requirements
• Hands-on experience with electronic documentation management systems and/or web-based data management systems
• Awareness of the clinical development process, including a deep understanding of the principles of Good Clinical Practice
• Solid grasp of regulatory requirements and relevant data standards
• Strong oral and written English communication skills
• Proficiency in Microsoft Office Suite

If You Have (Preferred Requirements)

• Experience with clinical trial management systems (CTMS)
• Familiarity with data validation and quality control processes
• Ability to work collaboratively in a team environment
• Strong problem-solving skills and attention to detail
• Experience using common AI tools, including generative technologies such as ChatGPT or Microsoft Copilot, to support problem solving and enhance productivity.
• Demonstrated curiosity for exploring how these tools can improve outcomes and understanding of responsible AI practices, including risk management and ethical use

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.

Medical 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.