Full-Time

Research Assistant 3

University of Miami

University of Miami

Research university in Coral Gables, FL

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Biology & Biotech (1)
Required Skills
Data Analysis

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Requirements
  • A high school diploma or equivalent/relevant experience, certification, or license is required.
  • At least 3 years of relevant experience is required.
  • The candidate must be able to learn new procedures, technologies, and protocols and adapt to changing priorities and work demands.
  • The candidate must be able to work collaboratively with others and contribute to a team environment.
  • The candidate must be skilled in using office software, technology, and relevant computer applications.
  • The candidate must have strong written and verbal communication skills for interacting with colleagues and stakeholders.
Responsibilities
  • Plan and implement research experiments according to research protocols to assure high-quality scientific results in support of applicable project goals.
  • Participate in assessing the feasibility of implementing innovations.
  • Assess data trends and develop reports and presentations.
  • Support the initiation of new research by reviewing and synthesizing literature.
  • Oversee inventory of supplies and equipment and place orders in a timely fashion.
  • Assist in preparing scientific papers, reports, and manuscripts.
  • Recruit, screen, and enroll eligible participants for research studies.
  • Obtain informed consent and ensure that participants understand the research procedures.
  • Administer study-related procedures and interventions.
  • Conduct chart reviews and pre-screening to determine participant eligibility and coordinate basic clinical research protocols.
  • Coordinate 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.
  • Assist 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.
  • Perform moderate research tasks and adapt procedures for quality improvement under supervision.
  • Follow technical instructions for operating clinical research equipment and assist in troubleshooting operational issues.
  • Assist in monitoring and reporting adverse events to the Principal Investigator or supervisor, including events reported by participants.
  • Address adverse events according to protocol, advocate for participants, and maintain quality standards throughout the study.
  • Identify, report, and assist in resolving protocol deviations and unanticipated events.
  • Complete 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.
  • Adhere to University, unit-level, and department-specific policies and procedures and safeguard University and departmental assets.

The University of Miami is a private research university focused on education, discovery, and service, with undergraduate, graduate, and professional programs.

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