Research Study Coordinator 1-Medicine General (Internal)

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profile Job Location:

Memphis, TN - USA

profile Monthly Salary: Not Disclosed
Posted on: 4 days ago
Vacancies: 1 Vacancy

Job Summary

Description

Market Range: 08

Hiring Salary: $21.69/Hourly

THIS IS A GRANT FUNDED POSITION FUNDED UNTIL JANUARY 31 2028

JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under direction of the Principal Investigator the Research Study Coordinator 1 assists with participant recruitment informed consent baseline and follow-up data collection coordination with hospital pharmacy teams and delivery of health coaching using motivational interviewing techniques. The position involves close interaction with patients clinical staff and the research team to ensure fidelity to study protocols accurate data collection and adherence to ethical and regulatory standards.



Responsibilities
  1. Identifies potentially eligible patients through daily chart review and coordinates with hospital staff for referrals.
  2. Approaches screens and recruits eligible participants during hospitalization.
  3. Conducts the informed consent process in accordance with IRB-approved protocols.
  4. Coordinates with hospital pharmacies to ensure bedside medication delivery at zero copay for participants randomized to the intervention arm.
  5. Facilitates and monitors home delivery of medications post-discharge in collaboration with hospital couriers and outpatient pharmacy services.
  6. Conducts 3- 6- and 12-month follow-up visits and/or telephone assessments using standardized questionnaires.
  7. Maintains accurate and timely documentation of all participant contact and study activities in REDCap.
  8. Provides individualized health coaching to participants using motivational interviewing techniques focused on medication adherence and chronic disease management.
  9. Conducts and documents semi-structured qualitative interviews to assess patient experiences with the intervention.
  10. Performs other duties assigned.


Qualifications

EDUCATION:Bachelors Degree. (TRANSCRIPT REQUIRED)

EXPERIENCE: One (1) year of clinical research experience; OR Masters Degree will be accepted in lieu of experience.

KNOWLEDGE SKILLS AND ABILITIES:

  • Strong interpersonal and communication skills.
  • Knowledge of research ethics patient confidentiality and informed consent procedures.
  • Familiarity with motivational interviewing or other patient engagement strategies preferred.
  • Ability to coordinate activities across multiple departments (e.g. pharmacy nursing case management).
  • Proficiency with electronic data capture systems such as REDCap and Microsoft Office.
  • Excellent organizational skills and attention to detail.
  • Previous recruitment experience.



Required Experience:

IC

DescriptionMarket Range: 08Hiring Salary: $21.69/HourlyTHIS IS A GRANT FUNDED POSITION FUNDED UNTIL JANUARY 31 2028JOB SUMMARY/ESSENTIAL JOB FUNCTIONS: Under direction of the Principal Investigator the Research Study Coordinator 1 assists with participant recruitment informed consent baseline and fo...
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