Clinical Research Careers with KRGI 

in United Kingdom of Great Britain

REGIONAL CLINICAL RESEARCH ASSOCIATE in london area

FOR CLINICAL RESEARCH STUDY OF Serotonin  Receptor Inhibitor (determination of safety and efficacy) 

Our client an international pharmaceutical research company is planning to run a clinical trila in Great Britain.
As a CRA you will be overseeing the conduct of a clinical trials, working on complex, intensive projects, where an in-depth knowledge of ICH-GCP and SOP-s is highly beneficial.

These positions are field based within London area.

Responsibilities

• Assists in the preparation of protocols, CRFs, regulatory binders, physician brochures, and study manuals. 

• Assists in the preparation of regulatory submissions and in the preparation of interim and final study reports to Ethic Committee.  

• Performs study site identification, qualification, initiation, interim monitoring, and close-out visits in accordance with company SOPs.

• Maintains close communication with clinical sites to ensure adherence to protocol and regulatory requirements. 

• Monitors CRFs and source documentation, informed consent documents.

• Collects CRFs and other study related supporting documentation (e.g., Ethic Committee approvals and renewals, correspondence, X-rays, etc.) 

• Monitors regulatory binder. 
  Monitors drug accountability. 

• Identifies, tracks, and reports adverse events (AE). 

• Monitors queries generated by data management. 

• Completes and submits monitoring reports.
  
  
  Job requirements:

•  Education and training: Bachelor's degree in science or related field. 

• Two or more years experience in clinical site monitoring 

• Excellent working knowledge of Good Clinical Practice (GCP)

If you think you are the right person, don’t miss this opportunity, and send your CV now  to  hr6@krgi.org