Clinical Trials Nurse & Research Coordinator

HCA Healthcare, Inc.

Asheville (NC)

On-site

USD 70,000 - 95,000

Full time

14 days+

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Benefits offered by this job

Comprehensive benefits
Wellbeing support
Time away from work programs
Savings and retirement resources
Education support
Additional benefits

Job summary

Mission Health, part of HCA Healthcare, is seeking a Research Nurse to coordinate multiple clinical trial protocols at a hospital-based site in Asheville, NC. You will liaise with investigators, staff, and research personnel to build a strong foundation in human subject research.

You will enroll patients, review eligibility with physicians, verify informed consent, and ensure data accuracy across study forms and electronic systems. Flexibility to cover after-hours or weekends may be required.

Qualifications

  • Associate’s Degree required; Bachelor’s Degree preferred.
  • Active RN License required.
  • Knowledge of federal regulations and good clinical practices (GCP).
  • Knowledge of medical and research terminology.
  • Computer skills including clinical trial database, electronic data capture, MS Word or Excel.
  • Excellent verbal and written communication skills.
  • Ability to work independently in a fast-paced environment.

Responsibilities

  • Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements.
  • Work with the principal investigator to meet or exceed study enrollment.
  • Review study design and inclusion/exclusion criteria with physician and patient.
  • Ensure protection of study patients by verifying informed consent procedures.
  • Ensure data integrity by source document review and monitoring for missing data.
  • Maintain accurate records including regulatory documents and consent forms.
  • Enter data into CRFs or electronic data capture systems.
  • Coordinate shipments of drugs and devices as needed.
  • Report and follow up on adverse events as necessary.
  • Communicate protocol-related issues to study colleagues or manager.
  • Attend on-site meetings, investigator meetings, and CRC meetings as required.
  • Apprise PI and regional managers of study-specific issues for guidance.
  • Assist sponsor and US FDA audit teams.

Skills

RN License
Regulatory knowledge
Data entry
Communication

Education

Associate’s Degree
Bachelor’s Degree preferred

Tools

Clinical trial database
Electronic data capture
MS Word
MS Excel

Job description

Mission Health, part of HCA Healthcare, is seeking a Research Nurse to coordinate multiple clinical trial protocols at a hospital-based site in Asheville, NC. You will liaise with investigators, staff, and research personnel to build a strong foundation in human subject research.

You will enroll patients, review eligibility with physicians, verify informed consent, and ensure data accuracy across study forms and electronic systems. Flexibility to cover after-hours or weekends may be required.

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