Emory University
Emory University
Emory University ir pētniecības universitāte Atlantā, Džordžijas štatā, kuras akadēmiskās un profesionālās programmas aptver mākslu, dabaszinātnes, uzņēmējdarbību, tiesību zinātni un medicīnu. Universitātes darbība savieno izglītību ar veselības aprūpi un zinātnisko pētniecību, vienotā universitātes vidē apvienojot mācīšanu, zināšanu radīšanu un kalpošanu sabiedrībai.

Clinical Research Coordinator II – PFAS Study

Coordinate field operations for Emory University’s North Georgia PFAS exposure-reduction study. Responsibilities include participant visits and consent, questionnaires, biological specimens, and study records.

Apraksts

  • Oversee clinical trial administration and support the five-year North Georgia PFAS Study funded by NIEHS and NIH.
  • Coordinate on-site study operations in Floyd and Gordon counties.
  • Schedule and oversee study visits with participants.
  • Obtain informed consent, administer questionnaires, and screen participants.
  • Collect, process, manage, store, and ship biological specimens.
  • Maintain study records and conduct routine data quality checks.
  • Manage project databases, prepare study documents and flow sheets, and complete source records and case report forms.
  • Guide less experienced staff.
  • Assess participant eligibility and obtain consent in accordance with the study protocol.
  • Approve supply orders and equipment maintenance requests.
  • Support recruitment, interviews, and questionnaires.
  • Prepare case packages, track procedure scheduling and charges, and coordinate related services.
  • Check protocol compliance, review case report forms, verify source records, and attend sponsor monitoring meetings.
  • Prepare regulatory submissions.
  • Update the Research Project Manager and Emory University investigators on field operations.
  • Resolve operational problems and support consistent application of study protocols.
  • Build relationships with participants and community partners to support retention and community-engaged research.
  • Perform phlebotomy or diagnostic procedures when properly trained and credentialed.
  • Oversee clinical trial administration and support the five-year North Georgia PFAS Study funded by NIEHS and NIH.

Prasības

  • High school diploma or GED plus five years of clinical research experience; or two years of college in a scientific, health-related, or business administration program plus three years of clinical research experience; or LPN licensure plus two years of clinical research experience; or a bachelor’s degree in a related field plus one year of clinical research experience; or a master’s, MD, or PhD in a related field.
  • Clinical training must be tracked and monitored through Emory Healthcare under the Clinical Researcher credentialing category.
  • Knowledge of epidemiology and/or environmental health research, clinical research projects, and clinical trials.
  • Experience in community-based or clinical human-subjects research.
  • Experience collecting, processing, and/or shipping biological specimens.
  • Phlebotomy certification is preferred, or willingness to obtain it.
  • Ability to maintain accurate study records and ensure data quality.
  • Phlebotomy training or willingness to train is preferred.
  • Highly organized, proactive, and reliable, with willingness to work occasional nights or weekends.
  • Must live in, relocate to, or commute to Northwest Georgia.
  • Ability to work independently in a field-based research setting and collaborate with a broader team.
  • Ability to collect, store, and ship biological specimens, including urine and stool.
  • Ability to build and maintain trusted relationships with participants and community partners in Northwest Georgia.
  • Highly organized, proactive, and reliable, with willingness to work occasional nights or weekends.
  • Must live in, relocate to, or commute to Northwest Georgia.
  • Ability to work independently in a field-based research setting and collaborate with a broader team.
  • Ability to collect, store, and ship biological specimens, including urine and stool.

Priekšrocības

  • A remote workday may be available at the department’s discretion.
  • Study-funded occasional travel to Atlanta for team meetings or professional development.
  • Professional development activities.
  • Equal opportunity employment and consideration without discrimination.
  • Reasonable accommodations for qualified individuals with disabilities.

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