Neonatal Research Specialist — Part Time

University of Mississippi Medical Center

Jackson (MS)

On-site

USD 25,000 - 39,000

Part time

7 days ago
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Job summary

University of Mississippi Medical Center in Jackson, MS is seeking a Research Specialist - Newborn Medicine - Part-Time to coordinate and conduct research projects. You will manage recruitment, data collection, and retention of participants in line with study protocols and FDA guidelines.

You will ensure adherence to institutional policies, coordinate daily research activities, and maintain accurate records while communicating effectively with the research team and participants involved in

Qualifications

  • Bachelor's degree plus two (2) years related experience.
  • Knowledge of principles and procedures of clinical, population/health services, or translational research.
  • Strong verbal and written communication skills; ability to interact with diverse constituencies.
  • Ability to prepare and process data and biological/environmental samples using established protocols.

Responsibilities

  • Participates in planning, development, and implementation of research protocols.
  • Recruits, enrolls, and retains eligible research participants with proper documentation.
  • Provides basic study background and education to participants.
  • Oversees daily research activities and procedures, ensuring participant safety and data integrity.
  • Inputs data and maintains records for research.
  • Disseminates research information to faculty, staff, and investigators.
  • Ensures activities adhere to protocols, procedures, and safety standards.

Skills

Research coordination
Verbal & written communication
Interpersonal skills
Data handling
Compliance knowledge

Education

Bachelor's degree + 2 years related experience

Job description

University of Mississippi Medical Center in Jackson, MS is seeking a Research Specialist - Newborn Medicine - Part-Time to coordinate and conduct research projects. You will manage recruitment, data collection, and retention of participants in line with study protocols and FDA guidelines.

You will ensure adherence to institutional policies, coordinate daily research activities, and maintain accurate records while communicating effectively with the research team and participants involved in

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