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Clinical Trial Transparency Associate require at GSK Rx India

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Clinical Trial Transparency Associate require at GSK Rx India

GlaxoSmithKline Pharmaceuticals Ltd. (GSK Rx India) is one of the oldest pharmaceuticals company and employs over 5000+ people. Globally, we are a £ 27.4 billion, leading, research-based healthcare and pharmaceutical company. In India, we are one of the market leaders.

Post : Associate, Clinical Trial Transparency

Position Details
As Clinical Support Staff you will be responsible for working in collaboration with the Project Delivery Lead and Study Delivery Lead to provide operational and administrative support for projects and study delivery activities. You will also provide support on contract development for Intercompany Clinical Trial Agreements (ICTAs) and Service Agreements.

Job Description
• Ensure high quality and up-to-date information in planning and tracking tools for project and study level data
• Ensure consistency in study and project level information between the Clinical Project Tracking and other relevant databases using available reports
• Follow-up with study team members to resolve discrepancies as needed and escalate any issues to Study Delivery Lead (SDL) and Project Delivery Lead (PDL).
• Assist in preparing study/project reports and status, assist in compiling data in preparation of study/project presentations, and updates related to time, budget, and quality
• Coordinate Study Budget Breakdown (SBB) process and track SBB status from start to end
• Review budget actuals versus forecasts, monitor expenses on a regular basis, support monthly studies budget, and any cost management plan maintenance
• Provide support in resolution of deviations and issues in actual expenses and escalate as appropriate


• Support SDL and PDL for quality assessment, controls, inspections, and audits as required
• Prepare and/or customize study document templates according to study requirements
• Provide support to ensure documents needed for submission are available for the respective country
• Collect central study essential documents and conduct Level 1 Quality Control and maintain an overview of local study essential documents
• Provide an overview of the Financial Disclosure activities and cascade to study team
• File and archive central study essential documents and provide support for filing and archiving of local study essential documents

Candidate Profile
• Bachelor’s degree in General Sciences or Life/Health related Science Degree (consult manager on health related)
• Experience working in a pharmaceutical or scientific environment
• Project Management experience
• Scientific background and knowledge of clinical trails
• Detail-oriented and organized
• Systematical approach to problem solving
• Good time management skills with the ability to clearly identify priorities and manage multiple tasks
• Knowledge of basic finance and accounting principles to understand budget, invoices, cross-charges and expense reports
• Knowledge of Microsoft office tools with advanced Excel, MS project, eTrack, Documentum and SAP
• Excellent communication skills


Additional Information
Job ID :
284510
Location : Karnataka - Bengaluru
Industry Type : Pharma / Healthcare / Clinical research
End Date : 30th March, 2021

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