Pfizer Hiring Associate Data Manager – Clinical Data Sciences
Are you searching for Pfizer careers in Chennai, clinical data management (CDM) jobs, or associate data manager roles in clinical data sciences? Global biopharmaceutical leader Pfizer has announced a vacancy for the position of Associate, Associate Data Manager, Clinical Data Sciences within its Clinical Development & Operations (CD&O) division in Chennai, India.
This clinical data review, Electronic Data Capture (EDC) testing, e-data validation, Trial Master File (TMF) coordination, and query management vacancy operates under a full-time, on-premise model based at Pfizer's office in Chennai. The position is open to life sciences, pharmacy, biotechnology, or biomedical sciences graduates holding Bachelor's or Master's degrees. Candidates must possess at least 1 year of active clinical data management experience, with strong skills in data cleaning, review workflows, and standard data management software. To create an ATS-friendly resume highlighting your EDC database design, query logs, or clinical data standards proficiency, check our guide on how to apply for healthcare and pharma jobs online.
📋 Job Overview
- Company: Pfizer
- Position: Associate, Associate Data Manager, Clinical Data Sciences
- Job Requisition ID: 4960573
- Job Location: Chennai, Tamil Nadu, India
- Employment Type: Full-Time
- Work Mode: On-Premise
- Experience: 1 Year+
- Qualification: Bachelor's or Master's Degree in Life Sciences, Pharmacy, Biotech, Clinical Research, Biomedical, or healthcare disciplines
- Estimated Salary: ₹5,0,000 – ₹9,0,000 per annum (Approximate CTC)
💼 Key Responsibilities
- Clinical Data Review: Perform systematic data reviews, query management, and data cleaning activities within clinical databases.
- Database Testing & Design: Support design, testing, validation, and implementation of Electronic Data Capture (EDC) systems and clinical databases.
- E-Data Management: Manage data acquisition, e-data loading validations, e-data error checks, and database release activities.
- TMF Maintenance: Maintain study-specific documentation within the Trial Master File (TMF) and ensure inspection readiness.
- Regulatory Alignment: Support regulatory submission activities, standard audits, and data deliverables under strict SOP guidelines.
- Cross-Functional Collaboration: Partner with Clinical Data Sciences teams to execute data visualization, reporting, and clinical data standards.
To learn more about the distinction between data management systems and analytical programming tools, read our guide on Clinical SAS vs Clinical Data Management.
🎓 Required Qualifications & Skills
- Education: Bachelor's or Master's degree in Life Sciences, Pharmacy (B.Pharm, M.Pharm), Biotechnology, Clinical Research, Biomedical Sciences, or related healthcare fields.
- Experience: Minimum of 1 year of clinical data management (CDM) or clinical data operations experience.
- Systems Knowledge: Practical understanding of EDC systems (e.g., Medidata Rave, Oracle Clinical) and trial systems (eTMF).
- GCP Awareness: Knowledge of clinical trial development phases, regulatory standards, and ICH-GCP guidelines.
- Analytical Skills: Good logical reasoning, query tracking, data visualization, and documentation practices.
- Communication: Strong verbal and written English communication skills for collaborative global team dynamics.
To prepare for detailed clinical data review, database validation, and registry workflows, check out our guide on Clinical Data Management (CDM) Interview Questions.
🎁 Why Join Pfizer?
- Work for a global biopharmaceutical company dedicated to delivering breakthroughs that change patients' lives.
- Gain experience using state-of-the-art clinical databases, EDC systems, and data visualization tools.
- Structured professional development pathways and access to global clinical trials.
- Collaborative workplace culture with focus on employee development and learning.
To evaluate your skills in clinical operations and GCP tracking systems, practice with our interactive Clinical Trial Assistant Quiz.
📝 Resume Tips for Pfizer Candidates
- Mention Specific Databases: Explicitly name the EDC databases (like Medidata Rave, Oracle Inform, Veeva) you have experience with.
- Quantify Experience: Specify the number of studies you supported, queries managed, or database validation cycles you performed.
- Highlight TMF Tasks: If you filed documents or conducted QC checks for TMF, mention it under your clinical documentation skill sets.
💬 Pfizer Associate Data Manager Interview Questions
- Q1. What is the process of query management in clinical data management?
Answer Guidance: Query management involves identifying discrepancies during data review, generating a query in the EDC system to clarify the data point, routing it to the site coordinator, verifying the updated data once corrected, and closing the query to ensure database cleanliness. - Q2. How do clinical data managers ensure data privacy during clinical trials?
Answer Guidance: Data privacy is maintained by strictly anonymizing subject records. Data is uploaded into EDC using unique subject numbers (USUBJID) and initials, ensuring no personally identifiable information (PII) like name, phone number, or address is entered or visible in the system. - Q3. Explain what a Data Management Plan (DMP) is.
Answer Guidance: A DMP is a clinical study-specific document that details the data collection methods, database design guidelines, query management rules, external data integration pathways, quality control measures, and steps required to lock the database at study closeout.
📖 How to Apply?
Before submitting your application, please read our step-by-step guidance on how to navigate the Workday registration portal, fill out required forms, and format your application profile:
📄 Premium ATS Resume Builder Service
Want to build a professional ATS-friendly resume tailored for Clinical Data Management, Clinical Trial Operations, or Life Sciences roles? Message us directly on our LinkedIn Company Page with the phrase "I want Resume Builder Service", and our expert team will connect with you:
📲 Message Us on LinkedIn🚀 Direct Application Link
If you are ready with your documents, apply directly via the official Pfizer Workday careers portal:
Apply Online – Pfizer Careers (Job Requisition 4960573)📄 Try Free ATS Resume Analyzer & Builder
Want to build a professional, recruiter-ready resume before applying? Scan your ATS compatibility score and generate an optimized resume instantly:
🚀 Launch Free ATS Resume Tool❓ Frequently Asked Questions
Q. Is this Pfizer Clinical Data Management role remote?
No, this is a full-time, on-premise position based at Pfizer's office in Chennai, Tamil Nadu.
Q. What is the minimum experience required?
Candidates must have at least 1 year of clinical data management or clinical data operations experience.
Q. What qualifications are accepted for this vacancy?
A Bachelor's or Master's degree in Life Sciences, B.Pharm, M.Pharm, Biotechnology, Clinical Research, Biomedical Sciences, or related healthcare fields is accepted.
.png)
