Full-Time

Research Associate 2

SOM, Infectious Diseases

University of Miami

University of Miami

No salary listed

Company Does Not Provide H1B Sponsorship

Miami, FL, USA

In Person

Category
Lab & Research (2)
,
Required Skills
Ruby
Data Analysis
Requirements
  • Bachelor’s Degree in relevant field required
  • Minimum 2 years of relevant experience
  • Knowledge, Skills and Attitudes: Skill in collecting, organizing, and analyzing data.
  • Knowledge, Skills and Attitudes: Ability to recognize, analyze, and solve a variety of problems.
  • Knowledge, Skills and Attitudes: Ability to exercise sound judgment in making critical decisions.
Responsibilities
  • Performs specialized and complex experiments/studies.
  • Participates in the publication of significant research results.
  • Advances expertise through education, training, and research.
  • Writes extramural grants/proposals to gain support when appropriate.
  • Collects, prepares, analyzes, dissects, and evaluates specimens and tissue cultures.
  • Weighs and anesthetizes laboratory animals for experiments.
  • Operates sensitive and highly complex laboratory equipment.
  • Performs calculations to complete research test results.
  • Performs photography and dark room processing.
  • Participates in training sessions and workshops.
  • Adheres to University and unit-level policies and procedures and safeguards University assets.
  • Work with ID Research Unit Principal Investigator and Project Directors on on-going project needs active multisite & single site research studies to meet deliverable deadlines.
  • Identify, screen, and recruit eligible participants according to inclusion and exclusion criteria.
  • Obtain informed consent and explain study procedures to participants in a clear and ethical manner.
  • Support Clinical Research Coordinators in scheduling, preparing, and conducting participant study visits in alignment with study protocols.
  • Perform study assessments, including administering questionnaires, conducting interviews, and collecting clinical or behavioral data.
  • Interface with laboratory staff to ensure timely processing and tracking of samples.
  • Ensure completion and accuracy of all study visit forms, source documentation, and participant records.
  • Support retention strategies, including participant outreach, appointment reminders, and community engagement activities.
  • Maintain visit tracking logs and follow standardized operating procedures for visit documentation and quality control.
  • Maintain study binders, visit schedules, and regulatory documents in compliance with institutional and sponsor requirements.
  • Ensure participant confidentiality and data security according to IRB-approved procedures.
  • Participate in regular team meetings, trainings, and protocol reviews.

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