GSK
biopharma
DataLead,DataManagement
Neural analysis suggests this role is
optimal for Mid+ candidates.
“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.
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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