Employer Active
Responsiblity: • Overseeing thesmooth running of clinical trials. • Collecting,coding, and analyzing data obtained fromresearch. • Managing researchbudgets. • Informing participants about studyobjectives. • Administeringquestionnaires. • Monitoring researchparticipants to ensure adherence to studyrules. • Adhering to research regulatorystandards. • Adhering to ethicalstandards. • Maintaining detailed records ofstudies as per FDA guidelines, including things such as drugdispensation. • Liaising with laboratoriesregarding findings. • Participating in subjectrecruitment efforts. • Ensuring that thenecessary supplies and equipment for a study are in stock and inworking order. • Engaging with subjects andunderstanding their concerns.
Full Time