Research Project Coordinator-Preventive Medicine

University of TennesseeMemphis, TN

About The Position

This is a grant-funded position funded until May 31, 2027, with potential for extension based on funding availability. The Research Project Coordinator 1 supports the Principal Investigator in adolescent- and young adult-focused research. This role involves coordinating research studies and conducting related activities, with a focus on recruitment strategies, data collection, and retention for pilot intervention research, clinical trials, and capacity-building initiatives. The research areas include adolescent and young adult substance use disorder treatment, overdose prevention/response, and reproductive health, with an emphasis on community-based participatory research and youth participatory action research.

Requirements

  • Bachelor’s Degree in Biological Sciences, Psychology, Statistics, Literature or a related field.
  • Two (2) years of research experience; OR a combination of education and experience to equal six (6) years.
  • Ability to work independently and with a study team.
  • Highly developed organizational skills.
  • Effective time management skills are necessary to balance responsibilities.
  • Ability to understand quantitative and qualitative data collection techniques.
  • High level of interpersonal and communication skills.
  • Ability to effectively use Microsoft Office.
  • Ability to interact with adolescents and young adults with respect, compassion, and engagement.
  • Ability to treat members of the recovery community with respect, compassion, and engagement.

Nice To Haves

  • Master’s Degree preferred.

Responsibilities

  • Implements a multifaceted, weekly recruitment plan.
  • Problem solves recruitment issues; tracks recruitment strategies progress.
  • Oversees participant scheduling and coordinate with study staff and local community partners.
  • Screens patients for eligibility; coordinates, confirms, and documents distribution of participant incentives.
  • Oversees adherence to protocol, including informed consent, collection of measurements, and data entry.
  • Performs research interviews, interventions, fidelity-related observations and creates associated documentation.
  • Contributes ideas and suggestions for all phases of the project.
  • Utilizes statistical and database management software to analyze data and prepare summary narrative reports, tables, graphs, and figures.
  • Assists in the design of studies by reviewing proposals to determine research methods best suited to study objectives.
  • Monitors and analyzes data weekly to ensure no changes to the protocol are needed to improve retention or recruitment efforts.
  • Gathers and updates materials needed for grant, reports submissions and other investigator-related activities.
  • Plans, directs, and coordinates activities.
  • Negotiates contracts, monitors budgets, and purchases equipment.
  • Performs other duties as assigned.
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