Clinical Trial Assistant

 
Location: Irvine, California
Posted On: 3/14/2017
Job Code: ClinicalTA2828
Print
ALL ALL ALL
 
Job Description
 
Responsible for supporting the Clinical Trial Management/operational study team to manage the various aspects of the operational execution and delivery of quality studies, including in process quality control activities. activities.

II. PRIMARY JOB RESPONSIBILITIES:
Primary responsibilities of this position include:
• Supports the Clinical Trial Management/operational study teams in the execution and delivery of studies
• Support study feasibility activities and perform database/web searches for sites as needed. Work closely with the Site Start Up (SSU) and ensure all study related regulatory and financial documents are collected and reviewed in support of study activation.
• Organize and maintain project working files and track critical documents. Report discrepancies to the appropriate clinical team member in a timely manner.
Basic knowledge of drug development and FDA GCP/ICH regulatory guidelines is a plus
Supervision Received: Supervised by Clinical Trial Manager, Clinical Operations; Mentored by, and receives direction for specific study activities from Clinical Trial Manager
Category:Non-IT  code:new
 
 
Job Requirements
 
 
EDC
Internal:
• Clinical Document and Information Center (CDIC)
• Contracts Management
• Site Start Up
• Study team members
• Informatics
External:
• Sites
• Vendors
• IRB
 

Not Ready to Apply?
Contact Details
 
Recruiter
Vishal Singh
 
Phone
 
E-mail Address
 
LinkedIn
https://www.linkedin.com/in/vishal-singh-34bb6b105