GSK

biopharma

Manager,ClinicalDataManager

Mumbai, Maharashtra, India FULL TIME
Market Sentiment
HIGH DEMAND

Neural analysis suggests this role is
optimal for Manager candidates.

The Brief

“Manager, Clinical Data Manager at GSK. Skills: Clinical Data Management, Data Management, Data Validation. Accountable for end-to-end DS&M study activities. Define and execute Data Management Strategy”

What You'll Achieve.

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

Industry & Context.

biopharma
Problems you'll solve

Risk Management; Mediates and solves issues related to DM study deliverables

What They're Looking For.

Must Have

Clinical Data Management, Clinical Development, Clinical Information Systems, Clinical Trial Designs, Data Management, Data Validation, Risk Management, Data Analysis

What You'll Do.

Accountable for end-to-end DS&M study activities

Define and execute Data Management Strategy

Manage interim and final cleaned database lock

Archive DM documents in eTMF

Archive study database

Provide clinical data to study site

Manage complex studies

Lead day-to-day DS&M operational activities

Act as member of study core team

Single point of contact for DM study activities

Conduct sponsor oversight of FSP/FSO activities

Ensure training on protocol to FSP resources

Provide DM operational input into study design

Provide reports and status updates

Oversee and provide input to budgets

Create or review study level timelines

Promote implementation of clinical data standards

Act as first point of escalation for DM study issues

Ensure DM study deliverables compliance

Develop and maintain professional relationships

Act as mentor for junior DS&M team members

Act as Subject Matter Expert for new processes

Support implementation of data standards

Support implementation of new systems

Support vendor quality assessments

Support audits and inspections

How You'll Work.

Team & Collaboration

Act as member of the study core team; Develop and maintain excellent professional relationships with study team; Act as mentor for junior members of the DS&M team

Communication Scope

Communication; Influencing Without Authority; Stakeholder Management

Process & Methodology

Manage complex studies, Create or review study level timelines, Ensures teams adhere to timelines

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: * 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. * Accountable for one or several complex studies and has the ability and experience to manage the delivery of any type of study (different therapeutic areas, complex/unusual early phase setting, new/unusual indication, pivotal/Phase III and efficacy studies, clinical as well as epidemiology studies). * 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 a study outsourced through a DM Functional Service Provider (FSP) or Full Services Outsourcing (FSO), conducts & documents sponsor oversight of the end-to-end FSP/FSO study related activities and 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. * May oversees and provides input to the development of budgets forecasts for FSP and FSO contracts. * 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

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