. Collects, verifies, organizes, completes and records clinical information and data in case report forms. Performs the following.... Acts as liaison in support of pharmaceutical and investigator initiated clinical protocols. May participate in site...
, verifies, organizes, completes and records clinical information and data in case report forms. Performs the following data.... Acts as liaison in support of pharmaceutical and investigator initiated clinical protocols. May participate in site...
as the primary liaison to the Physician Investigator, the patient, the hospital and the company or government sponsor. The... assessments, blood draws, medication administration, etc. Complete source documentation and case report forms according to IRB...
) on communicable disease issues. Sexually Transmitted Disease (STD) general: Coordinates care provision, case and contact... with all mandatory training requirements. Lead and guides non-professional staff, i.e. Health Technician/Disease Investigator...
) on communicable disease issues. Sexually Transmitted Disease (STD) general: Coordinates care provision, case and contact... with all mandatory training requirements. Lead and guides non-professional staff, i.e. Health Technician/Disease Investigator...
) on communicable disease issues. Sexually Transmitted Disease (STD) general: Coordinates care provision, case and contact... with all mandatory training requirements. Lead and guides non-professional staff, i.e. Health Technician/Disease Investigator...
) on communicable disease issues. Sexually Transmitted Disease (STD) general: Coordinates care provision, case and contact... with all mandatory training requirements. Lead and guides non-professional staff, i.e. Health Technician/Disease Investigator...
teams, internal management and coworkers. Create and write case study review with guidance for senior colleagues. When... for training, investigator meetings, monitoring responsibilities, corporate meetings, and educational seminars. Physical Demands...
as outlined in the study protocol(s). Completes case report forms data entry and maintains source documentation for all study... adverse events and deviations to the Investigator as well as the sponsor and IRB in accordance to their requirements...
as outlined in the study protocol(s). Completes case report forms data entry and maintains source documentation for all study... adverse events and deviations to the Investigator as well as the sponsor and IRB in accordance to their requirements...