# Data Lead at GSK

GSK is hiring a Data Lead for a remote role open to applicants in India. Level rates it Little AI ●○○○; you can [apply on GSK](https://jobsbylevel.com/go/e315e4c9-4860-40f8-9a3a-dc3665135e7e?utm_medium=ai-agent).

AI Level 1, AI centrality 33 out of 100. Remote (Bengaluru Luxor North Tower).

## Details

- Company: [GSK](https://jobsbylevel.com/companies/gsk)
- AI level: AI Level 1 (score 33 out of 100)
- Location: Remote (Bengaluru Luxor North Tower)
- Posted: November 11, 2026
- Apply: https://jobsbylevel.com/go/e315e4c9-4860-40f8-9a3a-dc3665135e7e?utm_medium=ai-agent
- Free CV review for this job: https://jobsbylevel.com/cv-review?job=data-lead-at-gsk-ffd564

## Description

Business Introduction At GSK, we have bold ambitions for patients, aiming to positively impact the health of 2.5 billion people by the end of the decade. Our R&D focuses on discovering and delivering vaccines and medicines, combining our understanding of the immune system with cutting-edge technology to transform people’s lives. GSK fosters a culture ambitious for patients, accountable for impact, and committed to doing the right thing, making sure that we focus our efforts on accelerating significant assets that meet patients’ needs and have the highest probability of success. We’re uniting science, technology, and talent to get ahead of disease together. Find out more: Our approach to R&D Position Summary The Data Lead is responsible for overseeing the end-to-end DS&M study related activities and is accountable for all Data Strategy & Management (DS&M) study deliverables in terms of quality & delivery to plan. Responsibilities Accountable for the end to end DS&M study related activities in terms of quality & delivery to plan which include: Electronic Case Report Form and (electronic) Diary Cards & other clinical outcome assessments Defining and executing the Data Management Strategy including data ingestion, cleaning & reconciliation Interim and final cleaned database lock Archival of all DM documents in the eTMF Archival of the study database and provision of clinical data to the study site For an in-house study, leads the day to day DS&M operational study related activities, acts as a member of the study core team and provides sponsor oversight to the Functional Service Provider (FSP) working on the study For a study outsourced through Full Services Outsourcing (FSO), conducts & documents sponsor oversight of the end to end FSO study related activities. Provides DM operational input into the study design, the protocol, study planning, study documents including the study risk register Provides reports, status updates, feedback and advice to key study stakeholders on study progress. Creates or reviews study level timelines for DM deliverables and ensures teams adhere to these Promotes the implementation of clinical data standards to increase consistency, efficiency & productivity Acts as the first point of escalation for all DM study issues. Understands, mediates and solves issues related to DM study deliverables and escalates as required to DM representative at Asset level Ensures DM study deliverables are in compliance with GSK SOPs and regulatory guidelines Develops and maintains excellent professional relationships with study team and other key stakeholders Basic Qualification Bachelor’s Degree, in scientific or business discipline· Post Graduate Degree in Scientific Discipline Previous Experience Required Pharma and/or CRO experience. Understanding of disease area. Understanding of laboratory data. Understanding of applicable ICH/GCP regulations and applicable GSK policies and SOPs Preferred Qualification Experienced in Clinical Data Management processes, standards and clinical systems Project Management Exposure to Veeva, InForm, Rave, e-Diaries, e-Source is an added advantage Proficient in Microsoft exce and validation methodology Basic knowledge of PL SQL, SAS is an added advantage Understanding of general data flow & database architecture concepts Good understanding of regulations including ICH-GCP, 21 CRF part 11, CDISC requirement Comprehensive understanding of clinical drug /Vaccine development process Knowledge of medical terminology, anatomy and physiology Certification: CCDM (if present) added advantage If you are excited about growing your career while making an impact on clinical data quality, we encourage you to apply. We look forward to hearing how you can bring clarity and commitment to our clinical data management team. Skills Why GSK? Uniting science, technology and talent to get ahead of disease together. GSK is a global biopharma company with a purpose to unite science, technology and talent to get

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