Clinical Data Coordinator

ICON plc is a world-leading healthcare intelligence and clinical research organisation. From molecule to medicine, we advance clinical research providing outsourced services to pharmaceutical, biotechnology, medical device and government and public health organisations. With our patients at the centre of all that we do, we help to accelerate the development of drugs and devices that save lives and improve quality of life. Our people are our greatest strength, are at the core of our culture, and the driving force behind our success. ICON people have a mission to succeed and a passion that ensures what we do, we do well.

Key responsibilities :

Understanding and adhere to all assigned ICON SOPs and working procedures
Ensure all work performed is of high quality, compliant with Good Clinical Practice, ICH Guidelines and all applicable laws and regulations.
Need Record all billable and non-billable time in the appropriate timesheet management system.
Review CRF / eCRF data for completeness, accuracy, and consistency via computerized edits and manual data checks
You need to perform 3rd Party reconciliation activities in a timely manner and according to SOPs and WPs
Ensure you will participate preparation of final study documentation.
Create and maintain study files in study documents

Required experience and qualifications:
Job Title : CDC II
Job location : Bangalore
Office based
No of years of experience: 3+ years of relevant exp in conduct phase
Education Qualification: Any life science graduation
Salary : As per Industry standards with attractive benefits
Skill set : candidate should have good exposure in conduct study and reconciliatio