Sr. Research Associate - Bascom Palmer Eye Institute; Miami, FL

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The University of Miami, Bascom Palmer Eye Institute has an exciting full time opportunity for a Research Associate 3 in Miami, Florida. The Sr. Research Associate 3, SOM conducts highly specialized and complex research in support of the division’s research goals and objectives and assumes responsibility for the successful operations of the laboratory. The incumbent also supervises the activities of all laboratory staff and users and serves as subject matter expert and mentor to less experienced staff.

• Contributes to basic and applied research activities by collecting and analyzing data.
• Understands and interprets research protocols and procedures.
• Maintains an overview of relevant research findings.
• Ensures all research is undertaken according to good research practice.
• Designs, evaluates, and implements methods and protocols for assigned research projects.
• Recommends purchase of new equipment for research projects.
• Writes scientific articles and manuscripts for publication and presentation.
• Oversees and ensures the safe handling of radioactive and hazardous materials.
• Prepares analytical reports relative to research data.
• Adheres to University and unit-level policies and procedures and safeguards University assets.

This list of duties and responsibilities is not intended to be all-inclusive and may be expanded to include other duties or responsibilities as necessary.

Master’s Degree in relevant field

Not Applicable

Minimum 3 years of relevant experience

• Appointees will support research activities at the University and work under the direction of a principal investigator, program director, or designee of the principal investigator or program director, such as Assistant Scientist or above.
• Appointees may be required to supervise Research employees.
• The appointee is responsible for study planning and design, writing SOPs for study tasks, and selecting and recruiting appropriate eligible study patients.
• The position must be able to handle the expanding workload of recent expansion of the number of gene therapy clinical trials as well as neuro-ophthalmology clinical trials.
• The position must be able to contribute to scientific peer-reviewed paper preparations include manuscript writing, revision, locating and citing appropriate references, prepare graphs and tables, and paper submission.
• The appointee is responsible for sample and data collection, development of research protocol, implementation of research protocol and monitoring participant adherence.
• Conduct interviews of patients and control individuals to explain the study, obtain informed consent, and record standardized information. Document eligibility and baseline data from interviews, patient clinic charts and medical records.
• Maintain IRB, HIPPA and other regulatory documents.
• Prepare and submit consent forms and annual reviews to IRB. Notify IRB of protocol amendments, safety reports/serious adverse events, etc. in compliance with applicable regulations.
• Ensure site compliance with the clinical protocol and research guidelines; assures subject rights, safety, and welfare are protected.
• Organize and maintain data collection and analysis systems. Ensure data integrity and consistency in computer database and written records.
• Establish/maintain contact with patients/participants, health care providers, and community agencies.
• Maintain constant communication with the study sponsors on the status of the operation.
• Update appropriate agencies regarding current status of research project.
• Perform ophthalmic testing (e.g. OCT/optical coherence tomography, GDx, etc.) on patients for research studies.
• Obtain papers & other material for grant proposal submission & scientific publication submission.
• Appointees may be expected to contribute to extramural proposals, publications and presentations relevant to…