Research Assistant 3
The University of Miami
Current Employees: If you are a current Staff, Faculty or Temporary employee at the University of Miami, please click here to log in to Workday to use the internal application process. To learn how to apply for a faculty or staff position, please review this tip sheet. The University of Miami/UHealth Department of Public Health has an exciting opportunity for a full time Research Assistant 3 to work in Miami, FL. The Research Assistant 3 explores innovations to research and strives to improve implementation and family outcomes. The Research Assistant 3 ensures compliance with University policies, rules, and regulations to meet federal, state, and local standards pertaining to safety and ethics. Core responsibilities:
Full time Employee Type:
Staff
- Plans and implements research experiments, according to research protocols, to assure high-quality scientific results in support of applicable project goals.
- Participates in assessing the feasibility of implementing innovations.
- Assesses data trends and develops reports and presentations.
- Supports the initiation of new research by reviewing and synthesizing literature.
- Oversees inventory of supplies and equipment and places orders in a timely fashion.
- Assists in the preparation of scientific papers, reports, and manuscripts.
- Adheres to University and unit-level policies and procedures and safeguards University assets.
- Seeking a Research Assistant with a background in clinical research. Responsibilities include patient screening and enrollment, data management, and implementation of research protocols. The ideal candidate will be flexible, detail-oriented, and accountable in supporting scientific and research activities.
- Maintains enrollment procedures in accordance with study protocols.
- Recruit, screen, and enroll eligible participants for research studies.
- Obtain informed consent and ensure that participants fully understand the research procedures. Administering study-related procedures and interventions.
- Conducts chart reviews and pre-screening to determine participant eligibility and coordinates basic clinical research protocols.
- Coordinates routine clinical study activities, including data collection and maintenance, planning study timelines, scheduling appointments and study visits, organizing meetings, and supporting project evaluation activities.
- Maintain accurate and timely documentation, including case report forms, medical records, and study logs.
- Assists in preparing progress reports and annual self-evaluations of performance.
- Collaborate with a multidisciplinary research team, including investigators, data managers, administrative staff, and community-based staff.
- Participate in team meetings and provide updates on study progress, issues, and outcomes.
- Assist with data entry and quality control for research data.
- Performs moderate research tasks and adapts procedures for quality improvement under supervision.
- Understands and follows technical instructions for operating clinical research equipment and assists in troubleshooting operational issues when they arise.
- Assists in monitoring and reporting adverse events to the Principal Investigator or supervisor, including those reported by participants.
- Addresses adverse events according to protocol, advocates for participants, and maintains quality standards throughout the study.
- Identifies, reports, and assists in resolving protocol deviations and unanticipated events.
- Maintains required skills and completes mandatory training related to safety, equality, responsible conduct of research, continuing education, and research competencies.
- Collaborate with a local sexual health community-based organization to receive training in delivering PrEP navigation services
- Adheres to department-specific policies and procedures and safeguards departmental assets.
- High School Diploma or equivalent/relevant experience, certification or license
- Minimum 3 years of relevant experience required
- Learning Agility: Ability to learn new procedures, technologies, and protocols, and adapt to changing priorities and work demands.
- Teamwork: Ability to work collaboratively with others and contribute to a team environment.
- Technical Proficiency: Skilled in using office software, technology, and relevant computer applications.
- Communication: Strong and clear written and verbal communication skills for interacting with colleagues and stakeholders.
Full time Employee Type:
Staff
Vacancy posted 3 days ago
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