ClinicalDataLead

**_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. **Skills** Clinical Development, Clinical Research, Clinical Trial Designs, Clinical Trial Management Systems (CTMS), Communication, Fostering Collabo