Clinical Study Coordinators are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
KEY RESPONSIBILITIES AND TASKS
· Adhere to Good Clinical Practices and the study protocols
· Ensure scientific integrity of data and protect the rights, safety, and well-being of patients enrolled in clinical trials
· Provide patient with written communication of their participation (i.e. copy of the signed informed consent)
· Meet with patient for each visit and maintain accessibility to discuss any questions/concerns regarding the study
· Schedule all patient research visits and procedures consistent with protocol requirements
· Complete and maintain case report forms, and review them against the patient’s medical record for completeness and accuracy
· Administer questionnaires/diaries/other patient material per protocol
· Ensure that non-serious and serious adverse events are properly documented and reported
· Manage communication with study vendors as needed
· Ensure the filing and maintenance of all study documents
· Schedule monitor visits and set up for monitoring visits prior to monitor’s arrival
· Act as a liaison between site staff and different departments
· Saudi residency is required
. Minimum Experience 1 year .
Job Type:
Full-time
Job Type: Full-time