This list contains only the countries for which job offers have been published in the selected language (e.g., in the French version, only job offers written in French are displayed, and in the English version, only those in English).
Works under the supervision of the Principal Investigator (PI), Director and other site personnel. Conceptually applies the research protocol to the clinical setting. Maintains appropriate documentation. Ensures studies are conducted according to company policies and applicable regulations.
Job Responsibility:
Develops in-depth understanding of each study protocol to ensure all aspects of the protocol are adhered to
Under supervision prepares and submits regulatory documents
In collaboration with the PI, identifies potential study participants
Obtains informed consent
Schedules subject visits
Prepares labs/tests per protocol
Responsible for study drug storage and drug accountability
Administers the investigational product
Monitors and evaluates patients’ condition
Consults with PI regarding administration of investigational product
Conducts routine assessments
Educates the subject about the study
Documents subject information
Meets with the study monitor to review data
Reviews all lab/tests with the physician
Reports subject’s progress, complaints and issues
Conducts ongoing assessments of the overall study execution
Notifies appropriate management of serious adverse events
Collects pre-study essential documents
Maintains the study file record
Maintains subject participant records
Provides a list of all study participants to management
Ensures appropriate storage of records pertaining to investigational product
Documents investigational product received dispensed, and returned
Completes clinical trials management system and case report forms
Attends Investigator Meetings
Requirements:
Bachelor’s Degree or an equivalent combination of education and experience
Graduate of a technical program in healthcare (e.g. LVN/LPN, Medical Assistant or Dialysis Technician) AA in Life Sciences or other health related field
2 to 5 years’ healthcare experience with Dialysis experience preferred
Research experience preferred
Willing to pursue CCRC or SoCRA certification when eligible
Current appropriate state licensure if applicable
Proficient with PCs and Microsoft Office applications