Login for faster access to the best deals. Click here if you don't have an account.

Associate - Clinical Trial Transparency Fresher's job

3 years ago   Medical & Healthcare   Bengaluru   641 views Reference: 6884
Job Details

Are you looking for an opportunity to support process improvement initiatives and shares best practices related to Clinical studies and projects? If so, this is the role for you.

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.

This role will provide YOU the opportunity to lead key activities to progress YOUR career. These responsibilities include some of the following:

  • 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

Selection Process: The selection will be on the basis of Interview.


To Proceed further click on - APPLY

If interested candidates can share your resume to mail ID mentioned in address.

Company Description
GSK is one of the world’s foremost pharmaceutical and healthcare companies, and we are proud to be part of an industry that improves the lives of others. We are embarking on a significant transformation journey that will support GSK in becoming a top-quartile data-enabled organisation