PHARMAFull-time
Associate Clinical Data Team Lead
BANGALORE (IN)ONSITEPOSTED: 8/18/2026
PHARMAFull-time
HIRING ORGANIZATIONTHERMO FISHER SCIENTIFICLife Sciences / Scientific Instruments / Biotechnology
ROLE DEFINITION & RESPONSIBILITIES
Core Responsibilities
Act as the assistant lead data manager across one or more clinical trial projects, supporting the Lead Data Manager through study setup, active data cleaning, and database close-out phases.
Apply project protocol requirements to operational clinical data workflows with minimal supervision.
Coordinate routine data cleaning tasks and delegate query management responsibilities across data management project team members to meet quality benchmarks and milestone timelines.
Assist in defining database specifications, supporting database build activities, and executing User Acceptance Testing (UAT) for eCRFs and edit checks.
Author, update, and maintain clinical data management study documentation (Data Management Plan, Data Validation Specifications, CRF Completion Guidelines).
Monitor operational study metrics, track data entry turnaround, and generate regular project-specific status reports for Project Managers and clients.
Track project deliverable risks, identify timeline bottlenecks, and support resource forecasting and hours tracking.
Deliver study-specific onboarding and procedural training to junior data associates on assigned clinical studies.
Technical & Domain Standards
Strong understanding of the Clinical Data Management lifecycle, Good Clinical Data Management Practice (GCDMP), and ICH-GCP guidelines.
Practical familiarity with Electronic Data Capture (EDC) systems (e.g., Medidata Rave, Oracle InForm, Veeva Vault CDMS).
Knowledge of edit check testing methodologies, User Acceptance Testing (UAT) execution, and clinical discrepancy resolution workflows.
Familiarity with clinical data standards, CDISC conventions, and strict regulatory compliance requirements for clinical trials.
Leadership & Cross-Functional Collaboration
Support the primary Lead Data Manager in risk management planning, governance discussions, and client status meetings.
Mentor and provide day-to-day procedural guidance to junior data management staff.
Collaborate closely with cross-functional project teams including Clinical Operations, Biostatistics, and Quality Assurance to maintain deliverable integrity.
Benefits & Total Rewards
Opportunity to work with a premier global leader in life sciences serving top pharmaceutical and biotech innovators.
Competitive entry-to-early career compensation structure with annual performance-linked incentives.
Comprehensive medical insurance coverage, employee assistance programs, and wellness resources.
Robust global learning, development, and career mobility pathways across clinical research services.
REQUIRED VERIFIED SKILLS
Clinical Data Management (CDM)
Electronic Data Capture (EDC)
User Acceptance Testing (UAT)
Data Cleaning
Query Management
Database Build
Edit Checks
ICH-GCP
Study Setup & Closeout
Data Management Documentation
COMPENSATION & REWARDS
₹4.5L - 8.5L per annum
ORGANIZATION CONTEXT & CULTURE
Thermo Fisher Scientific is a global leader in serving science, providing an extensive range of analytical instruments, laboratory equipment, reagents, consumables, software, and services. They partner with pharmaceutical and biotech companies, hospitals, clinical diagnostic labs, universities, research institutions, and government agencies. The company's mission is to enable its customers to make the world healthier, cleaner, and safer.
TEAM SIZE: 130,000+ employees
INDUSTRY: Life Sciences / Scientific Instruments / Biotechnology
RECOMMENDED TRAINING
1/5
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