Job Description
-Assist research team in all clinical trials and administer and enter all study data into electronic systems efficiently
-Maintain all data logs and ensure consistency in all data
-Plan and track all clinical activity and monitor all lifecycle of trials from conceptualization to implementation
-Train all staff on all protocol specification and assess local laboratory and prepare required documentation for same
-Assist all pharmacists and ensure appropriate clinical and drug supplies and provide an interface with all laboratory technicians and prepare reports for all events
-Administer individual trials on monthly basis and evaluate all documents for clinical processes and prepare all case reports and maintain an effective management database
-Evaluate all trial data and resolve all queries and assist all research scientists to resolve all medical issues and assist all audit teams
-Monitor all audits and evaluate all results, escalate issues to project manager if required
-Recommend improvements to increase efficiency of process and ensure compliance to all SOPS for clinical research and maintain all work as per code of conduct
-Provide update on all protocol issues and obtain approvals for all laboratory reports and manage all phone calls and provide status reports to all clients and update all patient lists
-Administer patient treatment processes and ensure compliance to all RECIST regulations and assign trials to all clinical processes
