Site Management
 

ICBio uses Oracle Clinical for Clinical Trial Management. We have an experienced work force with an effective project management team implementing our plan with utmost care. Prime emphasis is on maximizing Quality, Optimizing project budget, Meeting all time lines while always focusing to ensure all TATs from us and sites are met. We also support in IEC/IRB and RA submissions and Pre-study qualification visits. We provide customized team and focus on each project which works on study documents designed per client preference and approval with further inputs as required.

  

ICBio provides customized team and highly skilled work force for an effective Site Management.

ICBio organizes and ensures efficient site training with regular investigator meetings right from the study start and then through the conduct stage to ensure high quality of data so that queries are minimized and that they are effectively addressed. We also provide site related financial support in trial (Investigator fees, etc)

Our clients are always having latest updates with respect to their trials being conducted through ICBio.
 
Services under Site Management Include:
 
Providing National Network of ICH –GCP trained sites
Conduct of OPD-based and in-patient trials across all therapeutic areas, including specialty segments like oncology
Larger patient numbers as compared to traditional sites
Shorter time frames for study start up & recruitment
GCP-trained clinical research staff consisting of Principal Investigators, Research Physicians, Nurses, Clinical Research Associates, Clinical Research Coordinators, Clinical Data Coordinators, Medical Coders, Patient Recruitment Specialists & Administrators
Unique Patient Recruiting System –“Clinical relations” system both at the Hub and Sites
Centralized Feasibility, Contract Development & Budgeting, Project Management for sites, Clinical Relations & Quality Control
Customized teams
Effective Patient recruitment
Continuous interaction with clients through Regular planned / Adhoc meetings
Support designing, review and approval of study documents
Investigator management (Contracts, Fees, administration, etc)
Vendor Management (Lab, Scanning, Translation, etc)
   
 
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