Research Assistant 3

University of MiamiMiami, FL
Onsite

About The Position

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. 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.

Requirements

  • 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.

Nice To Haves

  • Background in clinical research
  • Flexible, detail-oriented, and accountable in supporting scientific and research activities.

Responsibilities

  • 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.
  • 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.

Benefits

  • medical
  • dental
  • tuition remission
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