PHARMAFull-time
Lab Data Analyst
KOLKATA (IN)ONSITEPOSTED: 8/31/2026
PHARMAFull-time
HIRING ORGANIZATIONIQVIAHealthcare Technology & Contract Research
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Manage end-to-end Laboratory Data Management (LDM) activities across the clinical study lifecycle, from study setup to database lock.
Perform data validation, reconciliation, and quality control checks on laboratory datasets prior to transmission.
Develop, review, and maintain data management documentation including specifications, data transfer agreements, and validation plans.
Execute Python-based data processing and automation tasks for ongoing studies and ad-hoc departmental projects.
Ensure compliance with SOPs, regulatory guidelines, and data standards across all deliverables.
Technical & Domain Expertise
Strong understanding of clinical data management processes and laboratory data workflows.
Working knowledge of SAS programming and Python for data manipulation and validation.
Familiarity with regulatory standards including FDA, ICH, ISO HL7, and GLP.
Experience with electronic data transfer systems and laboratory information systems.
Ability to manage data queries, discrepancies, and issue resolution across stakeholders.
Leadership & Business Impact
Act as Local/External Lab Lead for global studies, serving as the primary contact for clients, CRAs, and site monitors.
Provide technical and scientific guidance to internal teams and laboratory stakeholders.
Manage timelines, escalate risks, and ensure high-quality delivery within agreed SLAs.
Train and mentor junior team members and support cross-functional collaboration.
Benefits & Total Rewards
Opportunity to work on global clinical trials and high-impact healthcare data.
Exposure to advanced data systems and regulatory frameworks.
Structured career progression within IQVIA's global data science and clinical operations ecosystem.
Access to learning platforms, certifications, and internal mobility programs.
REQUIRED VERIFIED SKILLS
Clinical Data Management
Laboratory Data Management
SAS Programming
Python
Data Validation
GLP
FDA Regulations
ICH Guidelines
Data Reconciliation
Clinical Research
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
For 2–5 years experience in IQVIA, compensation typically ranges from ₹5–10 LPA depending on technical expertise in SAS/Python and domain experience. Additional benefits may include performance bonuses, health coverage, and access to global career mobility programs.
ORGANIZATION CONTEXT & CULTURE
IQVIA is a leading global provider of advanced analytics, technology solutions, and contract research services (CRO) to the life sciences industry. The company helps pharmaceutical, biotech, and medical device clients accelerate the development and commercialization of new medical treatments through its extensive data, technology, and human expertise. Their offerings span from clinical trial design and execution to real-world evidence and commercial effectiveness.
TEAM SIZE: 87,000+ employees
INDUSTRY: Healthcare Technology & Contract Research
EXPECTED CAREER ROADMAP
This role opens pathways into advanced Clinical Data Management, Data Science in Clinical Trials, or specialized roles such as Clinical Data Lead, Biometrics Analyst, or Data Standards Expert. With experience, professionals can transition into leadership roles managing global trials or move laterally into biostatistics, regulatory data strategy, or real-world evidence analytics.
APPLICATION ADVISORY
Highlight hands-on experience in SAS/Python and clinical data workflows. Be ready for technical assessments involving data validation logic and scenario-based questions. Demonstrate understanding of regulatory standards (ICH, FDA) and emphasize attention to detail and quality control experience.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
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