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Patient RegistrationPosted 21 days ago

Soc/Clin Research Assistant

Full-time
On-site
Entry level
Competitive
Posted 21 days ago

The University of North Carolina at Chapel Hill seeks a Research Assistant to support the startup and management of clinical trials. The role involves patient interaction, trial data and query management, regulatory documentation, and study supply inventory.

Higher Education

Posted
21 days ago
Source
unc.peopleadmin.com
Sector
Healthcare

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Responsibilities

  • Assisting with the startup and management of clinical trials
  • Reviewing and understanding research protocols
  • Obtaining clinical trial data
  • Interacting with clinical trial patients
  • Answering trial queries
  • Registering patients in EPIC / CRMS for accurate billing
  • Submitting patient data
  • Maintaining and organizing data for regulatory compliance
  • Preparing ethics board applications
  • Maintaining study supply inventory
  • Following detailed instruction outlined by the research team
  • Acting independently within the scope of the clinical trial and instruction from the principal investigators
  • Completing related training such as Human Research Participant Protection and GCP training

Qualifications

  • Bachelor's degree; or equivalent combination of training and experience
  • All degrees must be received from appropriately accredited institutions

Preferred

  • Prior experience with research, Epic, and IRB

Required skills

EpicInstitutional Review Board (IRB)

Full job description

The University of North Carolina at Chapel Hill seeks a Research Assistant to support the startup and management of clinical trials. The role involves patient interaction, trial data and query management, regulatory documentation, and study supply inventory.

Higher Education

  • Insider Connection @Carolina Population Center
  • 2 email credits available today
  • Beyond your network
  • Margaret Swingler
  • Training Manager
  • From your previous company
  • Find More Connections
  • from your School
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Responsibilities

  • Assisting with the startup and management of clinical trials
  • Reviewing and understanding research protocols
  • Obtaining clinical trial data
  • Interacting with clinical trial patients
  • Answering trial queries
  • Registering patients in EPIC / CRMS for accurate billing
  • Submitting patient data
  • Maintaining and organizing data for regulatory compliance
  • Preparing ethics board applications
  • Maintaining study supply inventory
  • Following detailed instruction outlined by the research team
  • Acting independently within the scope of the clinical trial and instruction from the principal investigators
  • Completing related training such as Human Research Participant Protection and GCP training

Preferred

  • Prior experience with research, Epic, and IRB

Benefits

  • A wide range of professional training opportunities for career growth, skill development and lifelong learning
  • Numerous retail and restaurant discounts
  • Savings on local child care centers
  • Special rates for performing arts events
  • The Carolina Population Center (CPC) is a community of outstanding scholars and professionals associated to create new knowledge about population size, structure, and processes of change.
  • Chapel Hill, North Carolina, US
  • https://www.cpc.unc.edu
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Qualifications

  • Bachelor's degree; or equivalent combination of training and experience
  • All degrees must be received from appropriately accredited institutions
  • Prior experience with research, Epic, and IRB

Required skills

  • Epic, Institutional Review Board (IRB), Research Experience

Preferred skills

  • Prior experience with research, Epic, and IRB

Experience

  • Entry level

Job details

Employment type

Full-time

Seniority level

Entry level

Date posted

Oct 23, 2026

Work mode

On-site

Job source

unc.peopleadmin.com

Company

Patient Registration

Healthcare

  • United States
  • Healthcare

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