Performs study-related procedures such as physical examinations, informed consent, subject history, adverse events, test article handling, appointment scheduling, records review, treatment coordination, collecting vital signs, and subject health assessments.
December 03, 2022
Provide very good communication skills with patients and research staff regarding medical or psychosocial changes in the targeted renal transplant recipients that are currently or may be eligible for subject enrollment in the clinical pharmacology study.
December 17, 2022
Develops the need for and maintains an awareness of available resources, and makes recommendations to Medical Center management regarding needs, distribution or redistribution of these resources to include equipment, staffing, and space.
January 17, 2023
Demonstrated knowledge of adult learning, organizational behavior, and instructional design systems, required.
January 30, 2023
Participates in the review of source data and/or data listings of safety data, including adverse experiences, laboratory data, and vital signs data to establish the presence or absence of abnormal trends, and if noted, follow-up as appropriate with the clinical team, project team sponsor, investigator and regulatory agencies.
February 26, 2023
Assist with writing reports of research activities and results/outcomes for submission to required government organizations and preparing manuscripts of research activities and results/outcomes for publication as assigned by Chief, Division of Medicine.
March 07, 2023
Create complex strategies to develop the franchise or product and successfully articulate this to various constituents such as governance committees, project teams, clinical sub-teams, and other senior management to build enthusiasm, passion and commitment.
April 25, 2023
