Clinical Research Coordinator – Patient Data & Trials

Carolinas Medical Center

Charlotte (NC)

On-site

USD 35,000 - 52,000

Full time

3 days ago
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Benefits offered by this job

Paid Time Off
Health and welfare benefits
Educational Assistance Program
Retirement plan with employer match

Job summary

Advocate Health in Charlotte, NC seeks a Research Assistant to support academic vaccine trials. You will screen patients, collect and verify data, obtain consent, and maintain study records. The role requires attention to detail and teamwork in a clinical research setting.

Responsibilities include data entry, specimen processing coordination, and collaboration with sponsors to schedule visits. Some travel between sites may be required; familiarity with GCP/ICH guidelines is helpful.

Qualifications

  • Knowledge of medical terminology.
  • Proficiency in Microsoft Office (Word, Excel, Teams).
  • Excellent written and verbal communication; able to work in a team.
  • Ability to understand and communicate research protocol requirements.

Responsibilities

  • Screen for research trials and gather patient information to complete case report forms.
  • Review medical and database records to identify potential subjects for inclusion; obtain consent and register patients.
  • Enter and maintain patient and study information in electronic systems.
  • Maintain records of receipt, inventory and distribution of research materials.

Skills

Medical terminology
Computer skills
Communication
Attention to detail

Education

Associate's Degree in Health Science or related field

Job description

Advocate Health in Charlotte, NC seeks a Research Assistant to support academic vaccine trials. You will screen patients, collect and verify data, obtain consent, and maintain study records. The role requires attention to detail and teamwork in a clinical research setting.

Responsibilities include data entry, specimen processing coordination, and collaboration with sponsors to schedule visits. Some travel between sites may be required; familiarity with GCP/ICH guidelines is helpful.

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