Under the supervision of the Research Analyst, completes regulatory and administrative tasks for multiple research studies, including clinical trials, observational studies, and registry or biorepository research studies conducted within the Ocular Melanoma Center or Clinical Trials Group. Supports research team (investigators, research associate, research analyst and study coordinators) responsible for studies/research projects as appropriate, including but not limited to study initiation, patient enrollment, and ongoing data management activities. Working with the equipment technician and research team, maintains equipment, supplies inventory, and other materials used for the research biorepository.
Requirements
Position requires a bachelor's degree, preferably in the biological or physical sciences. Knowledge of relational database (e.g., Paradox or Access), graphics, spreadsheets and other software packages (Word, Excel, Powerpoint) helpful. Experience working in a clinical research setting (1+ years) is desirable.
Individual must possess strong quantitative, organizational, and communication (verbal and written) skills. Must have the ability to coordinate and prioritize multiple job tasks, to complete responsibilities within strict timelines, and to work independently as well as part of a team.
