Part-Time

Research Support Specialist

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Customer Experience & Support (1)
Required Skills
Data Analysis
Requirements
  • Bachelor’s degree in relevant field
  • Minimum 2 years of relevant experience
Responsibilities
  • Researches, collects, analyzes, and synthesizes data and maintains databases.
  • Conducts quality assurance checks, reports on the status of research activities, and submits monthly activity logs for protocol.
  • Organizes and coordinates community working group meetings for protocol activities.
  • Serves as the primary point of contact for community partners and supervises and oversees research data collection at protocol venues in the community.
  • Reviews study progress, identifies areas of opportunity, and recommends solutions.
  • Prepares and updates study research procedures manuals.
  • Assists with the preparation of grant proposals by processing regulatory documents for all institutions and offices involved.
  • Contributes to the publication and presentation of significant results and writes and edits material for publication and presentation.
  • Maintains research files and responds to phone calls on the research study phone line.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.
  • Enrolling new patients to participate in clinical research.
  • Performs chart review/pre-screening activities for study participant eligibility and coordination of simple clinical research protocols. Maintains enrollment procedures according to the protocol.
  • Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, scheduling appointments and study visits, meeting scheduling, and project evaluation.
  • Performs moderate research tasks and adapts procedures for quality improvement under supervision.
  • Understands and follows technical instructions for operating clinical research equipment, and problem-solving when operational failures occur.
  • Assists in observing and informing the PI/supervisor of adverse events, including those reported by study participants.
  • Addresses adverse events per protocol, advocating for study participants and quality standards throughout the lifespan of the study.
  • Identifies, reports, and helps solve problems in protocol deviations and unanticipated occurrences.
  • Follows the appropriate fundamental requirements of all international, national, and local regulatory bodies.
  • Maintains requisite skills and mandatory training in safety, equality, responsible conduct of research, continuing education, and research competencies.
  • Prepare monthly progress reports and annual self-evaluation of performance.
Desired Qualifications
  • CITI Program: Human Subject Research, Group 1: Biomedical Researchers (HSR), and Conflict of Interest (COI) preferred

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