Glixy Raju

I am an enthusiastic, highly motivated professional in clinical research, specifically in drug development from phase I to IV trials in various therapeutic areas. I am dedicated to improving services with a positive mind-set. Building on my science background & project management skills, I have gained expertise and knowledge in clinical research management including feasibility, risk assessments, budgeting, setting up, conducting, monitoring and closing out of clinical trials in addition to regulations and governance of research, submission to regulatory bodies,  research materials, liaising with 3rd party contractors, reviewing trial finance and contracts. I am keen to work on roles, which would allow me to use and further develop my skills in the field of drug development for better health now and in the future.

The clinical research field has been my career focus for the past 5.2 year. I am experienced in immunology, oncology, and cardiovascular studies. Expert in start up, conduct and close out studies

Knowledge in ICH GCP, Medical terminology

experienced in working with Clinical data base- Medidata Rave, Inform

client management, vendor management

I have Good communication skill and Microsoft office platforms

Tmf filing, Sop management, documentation

Data validation,Data review, Data entry DMP, Metric creation, edit specification, UAT

MSc Health service management - University of Chester, Uk