Feasibility Support Assistant
ICON
Total des années d'expérience :1 years, 11 Mois
• iSprint: Registering investigators into database, adding them to surveys, Status updates, Creation of Communication templates, Sending Feasibility Questionnaires/ Confidentiality agreements electronically.
• ClickTools: Creation of Feasibility Questionnaires and report generation.
• e-Room: Maintenance of e-room (pdf prints, CRT tracker)
• Data Analysis: Extraction of reports from ClickTools and iSprint, extraction of investigator data to be registered for studies as per specific requirements (indication, region, etc.)
• Actively participated in administrative projects and initiatives as assigned, being able to make sound decisions based on available information in order to contribute to the success of the group and ICON.
• Network and collaborate with other professionals, attending and presenting at meetings both internally and globally.
Experience in Electronic Data Capture trials:
* Inform
* Inform Architecture
Form designing and test data for reports and mapping team
Played the role of trainee CRC as well as Business Management Associate. Got detailed knowledge on:
• SMO and Clinical Trials Management.
• Informed consent procedure.
• Managed various employees working for the SMO in hospitals.
• Different documents involved in clinical trials
Completed Post Graduate Diploma in Clinical Research and Data Management Worked with Quintiles and ICON for a duration of 15 months