GSK

biopharma

DataLead,DataManagement

Chandigarh, India FULL TIME Remote Friendly
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Mid+ candidates.

The Brief

“Data Lead, Data Management at GSK. Skills: Data Management, DS&M study related activities, Data Management Strategy, DM sponsor oversight, DM operational input, DM study issues resolution, compliance with GSK SOPs and regulatory guidelines. Accountable for the end-to-end DS&M study related activities in terms of quality & delivery to plan. Defining and executing the Data Management Strategy including data ingestion, cleaning & reconciliation”

What You'll Achieve.

quality & delivery to plan; database lock; provision of clinical data; adherence to timelines; increase consistency, efficiency & productivity; compliance with GSK SOPs and regulatory guidelines

Industry & Context.

biopharma
Problems you'll solve

Understands, mediates and solves issues related to DM study deliverables

What They're Looking For.

Must Have

end-to-end DS&M study related activities in terms of quality & delivery to plan, Electronic Case Report Form, vendor data, and 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, leads the day-to-day DS&M operational study related activities, acts as a member of the study core team, single point of contact for all the DM study related activities & matters, conducts & documents DM sponsor oversight of the end-to-end FSP study related activities, ensures training on the protocol to the FSP resources working on the study, 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

What You'll Do.

Accountable for the end-to-end DS&M study related activities in terms of quality & delivery to plan

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

Leads the day-to-day DS&M operational study related activities

Acts as a member of the study core team

Single point of contact for all the DM study related activities & matters

Conducts & documents DM sponsor oversight of the end-to-end FSP study related activities

Ensures training on the protocol to the FSP resources working on the study

Provides DM operational input into the study design

study documents including the study risk register

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

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

How You'll Work.

Team & Collaboration

acts as a member of the study core team; Develops and maintains excellent professional relationships with study team and other key stakeholders; Provides reports, status updates, feedback and advice to key study stakeholders on study progress

Communication Scope

Provides reports, status updates, feedback and advice to key study stakeholders on study progress; Develops and maintains excellent professional relationships with study team and other key stakeholders

Process & Methodology

Creates or reviews study level timelines for DM deliverables and ensures teams adhere to these, study planning

Full Job Description

**_Key Responsibilities:_** • Accountable for the end-to-end DS&M study related activities in terms of quality & delivery to plan which include: o Electronic Case Report Form, vendor data, and other clinical outcome assessments. o Defining and executing the Data Management Strategy including data ingestion, cleaning & reconciliation. o Interim and final cleaned database lock o Archival of all DM documents in the eTMF. o 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 is the single point of contact for all the DM study related activities & matters. • For study outsourced through a DM Functional Service Provider (FSP), conducts & documents DM sponsor oversight of the end-to-end FSP study related activities and ensures training on the protocol to the FSP resources working on the study. May oversee Full Service Outsourced (FSO) studies. • 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. **Why GSK?** **Uniting science, technology and talent to get ahead of disease together.** GSK is a global biopharma company with a purpose to unite sc

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