Clinical Research Coordinators
We are looking for Clinical Research Coordinators, whose responsibilities include:
Responsible for the integrity and overall quality of assigned clinical research trials
Excellent admin skills (efficient management of all communications & office organization with sound multitasking capabilities)
Flexibility to be able to shift and reprioritize tasks as needed or directed by the management team
Scheduling trial participant visits in coordination with limited and varied physician investigator availability
Interviewing research study participants, obtaining informed consents, & completing relevant participant scales and histories
Dispensing/collecting study medication and providing accurate Investigational Product accountability
Collecting, organizing, and timely entering of data into EDC/CRF portals
Understanding ICH & GCP regulations & maintaining regulatory compliance for the trial site - attention to detail a must.
Strong technical expertise with Microsoft Office products (particularly Word, Outlook, Excel), Windows 7+ & fast typing skills