Provide support to the Client Sponsored and Supported R&D Trials across all therapeutic area.
Organize study start-up teleconferences with study team
Assist in study start-up activities and ensure compliance for the Drug Shipment as per client SOP's.
Update and maintain the data with accuracy and integrity within all relevant client study systems.
Supporting client Clinical Study team to meet urgent deliverables ensuring inspection readiness.
Assist the study teams in the close out activities to ensure compliance to SOP and effective study closure.
Compilation and generation of Clinical Study Report Modular Appendices.
Manage and Archive essential documents as per client TMF SOP.
Ensure the process KPI defined are met for the study.
Organize and participating in all appropriate meetings with client and stakeholders.
Employement Category:
Employement Type: Full time Industry: Pharmaceutical Functional Area: Pharmaceutical Role Category: Clinical Research Associate Role/Responsibilies: Clinical Study Support
Contact Details:
Company: Golden Opportunities Location(s): Chennai