Associate Data Manager, Clinical Data Sciences – Pfizer
Location
Chennai, India
Job Type
Full-time (Hybrid)
Experience Required
0–3 years of experience in Clinical Data Management, Clinical Research, Clinical Operations, or related Life Sciences domains.
Fresh graduates with relevant knowledge and skills may also be considered.
Estimated Salary Package (Market Standard)
₹5.5 – ₹9 LPA (approx.), depending on qualifications, skills, and interview performance.
Job Overview
The Associate Data Manager supports clinical data management activities by ensuring the accuracy, quality, and integrity of clinical trial data. The role involves data review, query management, database validation, documentation management, and collaboration with cross-functional clinical teams to support the successful execution of clinical studies.
Key Responsibilities
Perform Data Monitoring and Management (DMM) activities, including data review and query management.
Investigate logic check flags and resolve clinical data discrepancies.
Support database design through documentation, testing, validation, and implementation.
Act as the first point of contact for Clinical Trial Management System (CTMS) queries and support.
Follow Standard Operating Procedures (SOPs) and established work practices.
Collaborate with Study Teams, Document Owners, and Trial Master File (TMF) teams to resolve documentation issues.
Ensure data quality, completeness, and compliance with regulatory requirements.
Participate in process improvement initiatives and special projects.
Maintain accurate clinical documentation throughout the study lifecycle.
Educational Qualification
Bachelor's degree (BA/BS) in Life Sciences, Pharmacy, Biotechnology, Nursing, Biomedical Sciences, or any relevant discipline.
Required Skills
Understanding of ICH-GCP (International Council for Harmonisation – Good Clinical Practice) guidelines.
Knowledge of the clinical development process and regulatory requirements.
Experience with electronic documentation management systems or web-based data management systems.
Proficiency in Microsoft Office Suite.
Strong verbal and written English communication skills.
Good analytical and problem-solving abilities.
High attention to detail and data accuracy.
Ability to work effectively in a collaborative team environment.
Preferred Qualifications
Experience with Clinical Trial Management Systems (CTMS).
Knowledge of data validation and quality control processes.
Familiarity with clinical data management workflows.
Experience using AI productivity tools such as ChatGPT or Microsoft Copilot.
Understanding of responsible AI practices, including ethical use and risk management.
Work Environment
Hybrid work model.
Collaborative and cross-functional global clinical research environment.
Who Should Apply
Freshers and early-career professionals interested in Clinical Data Management, Clinical Research, Clinical Operations, or Pharmaceutical Research.
Candidates looking to build a career in clinical trials, data management, and drug development within the pharmaceutical industry.
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