Clinical Data Analyst II
Company: Labcorp
Location: Bengaluru, Karnataka, India
Department: Clinical Data Management
Job Type: Full-Time
Work Schedule: Rotational Shift
JOB OVERVIEW
The Clinical Data Analyst II is responsible for managing clinical data cleaning, reconciliation, and query resolution activities for global clinical trials. The role involves collaborating with sponsors, CROs, and internal teams to ensure high-quality clinical data, timely database lock, and compliance with Good Clinical Practice (GCP). This position plays a key role in clinical data management, discrepancy management, client communication, and regulatory compliance throughout the clinical trial lifecycle.
KEY RESPONSIBILITIES
Clinical Data Management
Manage data cleaning activities for assigned clinical studies.
Develop and implement study-specific query management strategies.
Maintain clinical databases and ensure data accuracy.
Monitor data quality throughout the study lifecycle.
Ensure timely database lock readiness.
Data Cleaning & Query Management
Review and resolve clinical data discrepancies.
Generate, track, and manage data queries.
Maintain data cleaning schedules.
Perform data reconciliation before database lock.
Update databases according to study requirements.
Client & CRO Coordination
Liaise with sponsors and CRO Data Managers.
Act as the primary contact for data reconciliation activities.
Communicate with internal and external stakeholders.
Negotiate project timelines when required.
Ensure client expectations are met.
Data Analysis & Quality Assurance
Analyze clinical data inconsistencies.
Perform quality checks on data revisions.
Review database reports and identify issues.
Validate data according to GCP guidelines.
Ensure compliance with study protocols.
Cross-Functional Collaboration
Coordinate with clinical operations and other departments.
Lead discrepancy resolution until closure.
Support implementation of global data management processes.
Participate in process improvement initiatives.
Escalate critical issues impacting study timelines.
Regulatory & Compliance
Ensure compliance with Good Clinical Practice (GCP).
Review Statement of Work (SOW) against protocol requirements.
Support audit and inspection readiness.
Maintain accurate clinical documentation.
Follow Labcorp quality standards and SOPs.
EDUCATIONAL QUALIFICATIONS
Required
Bachelor's Degree in Science
Preferred
Master's Degree in Science
EXPERIENCE REQUIREMENTS
Required
Approximately 6 years of clinical research or clinical data management experience.
Preferred
Experience in Clinical Data Management.
Healthcare or laboratory industry experience.
Knowledge of medical terminology.
Uttar Pradesh :
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Kannur | Kochi | Malappuram | Thiruvananthapuram | Trivandrum |Pondicherry (Puducherry) :
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Rangpo |India :
Remote, India | Siliguri |Illinois :
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Europe | France | Latvia | Lendava | Leuven | Poland | Slovenia | Spain |Finland :
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Istanbul | Turkey |Norway :
Norway | NOrway |Romania :
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Carlow |Republic of Ireland :
Cork | Dublin | Limerick | Waterford |Ulster :
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Swords |Republic of China :
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China | Quarry Bay |Liaoning :
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Leiden |Netherlands :
Netherlands |Remote Australia :
Arkansas | Remote Australia |New South Wales :
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Queensland |Melbourne :
South Yarra |United Kingdom :
England | Harlow | Leeds | London | Maidenhead | Salt Lake City | Stevenage | Stirling | United Kingdom |North Yorkshire :
Harrogate |South Yorkshire :
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Canada |Quebec :
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Athens | Koropi |Greece :
Greece |North Island :
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Manila |Croatia :
Croatia |Zagreb :
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Tallinn |Hà Nội :
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Japan | Saitama |Tokyo :
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Oulu |Southwest Finland (Varsinais-Suomi) :
Turku |Remote Korea :
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Kyiv |Lima Region :
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Midrand | South Africa |Nišava District :
Niš |Bohemia :
Prague |Chile :
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