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The University of Miami/UHealth Department of Public Health has an exciting opportunity for a full time Research Analyst to work in Miami, FL.
The Research Analyst prepares data, conducts statistical analysis and summarizes results for a variety of research projects.
Core responsibilities:
Analyzes data and interprets research findings.
Identifies appropriate data sources to conduct and execute analyses.
Verifies accuracy and internal consistency of reports, including required state and federal reports.
Ensures proper technical documentation and preparation of tabular and written reports and gives oral presentations.
Completes surveys and reports, discipline-specific accreditation, and admission and grant proposals.
Provides feedback and assistance on honing conclusions and recommendations into actionable findings.
Adheres to University and unit-level policies and procedures and safeguards University assets.
Department Specific Functions:
Participates in the management of assigned clinical trials within the Department of Epidemiology and Health Sciences. Responsibilities include conducting survey interviews, distributing interview workload, abstracting, assembling, and organizing research data while monitoring the clinical course of patients entered into research protocols. Participates in developing protocols with a particular focus on data collection through telephone surveys. Maintains a working knowledge of all assigned protocols to ensure the validity of clinical research data. Verifies patient eligibility, develops, maintains, and/or monitors case report forms or individual patient research charts, and enters clinical findings into a study-related database. Prepares reports on individual patients or a study population in response to investigator requests.
Protocol Management: Identifies, recruits, and enrolls eligible patients, their families, and/or healthy control subjects onto specified Epidemiology research protocols.Administers questionnaires and self-report inventories to enrolled research participants (patients, parents, controls). Performs protocol-directed procedures under the supervision of the principal investigator and other study staff.Organizes and maintains a system for monitoring subjects enrolled in longitudinal studies and ensuring the collection of data in a timely manner.Prepares and organizes data to promote efficient computer entry.Demonstrates knowledge of Good Clinical Practice Guidelines, IRB review, reporting requirements, and regulatory affairs.Compiles, analyzes, and summarizes data and prepares reports for review by the principal investigator; makes recommendations for practical application of protocol. Participates in the development of protocol roadmaps or flow sheets and may participate in the completion of reports and forms.
Data Management: Completes reports and forms and assists with developing tools to record data.Enters research data into the study database after finalizing the data with the principal investigator.Completes enrollment of patients.Monitors quality of data and applies knowledge of medical terminology and physiology to create entries. Participates in activities as a peer reviewer.Assists with the development and/or design of tracking and analysis tools for assigned protocols.Adheres to guidelines regarding honest reporting of sensitive and confidential clinical and administrative information.Conceptualizes research studies and participates in the development of research designs and methodologies as well as the design of data collection instruments.Edits received questionnaires, records refusals, and assigns non-respondents to interviewers for tracing and/or telephone interview.
This list of duties…