Research Nurse

HCA Healthcare, Inc.; Asheville (NC); On-site; USD 70,000 - 100,000; Full time

Benefits offered by this job

Comprehensive benefits

Wellbeing support

Paid time off and leave programs

401(k) with match

Tuition and certification support

Other employee benefits

Job summary

Mission Health, part of HCA Healthcare, seeks a Research Nurse to coordinate clinical trials on site. You will work with investigators and staff to enroll patients, ensure informed consent, and maintain high-quality data across study tools.

You will review study designs with physicians, monitor adverse events, and support regulatory and audit processes while ensuring confidentiality and timely documentation in a fast-paced hospital setting.

Qualifications

• Associate degree required; bachelor’s degree preferred.
• Active RN license required.
• Knowledge of federal regulations and GCP.
• Knowledge of medical/research terminology.
• Computer skills including trial databases, EDC, MS Word/Excel.
• Strong communication and interpersonal skills.

Responsibilities

• Coordinate multiple research protocols and liaise with investigators, staff, and research personnel.
• Recruit, screen, enroll, and follow up with patients per protocol.
• Ensure informed consent procedures and protocol compliance.
• Maintain accurate CRFs and electronic data in data capture systems.
• Track shipments and study-related supplies; report adverse events.
• Ensure regulatory documents and source records are complete and organized.

Skills

Communication skills

Interpersonal skills

Organizational skills

Independent work

Team collaboration

Education

Associate’s Degree

Bachelor’s Degree preferred

Tools

Clinical trial database

Electronic data capture

MS Word

MS Excel

Job description

Do you have the career opportunities you want with your current employer? We have an exciting opportunity for you to join Mission Health which is part of the nations leading provider of healthcare services, HCA Healthcare.

The Research Nurse is responsible for coordinating multiple research protocols and serving as a liaison with local investigators, clinical staff, and research personnel. Under direct supervision, this individual will mature in their understanding of research operations and regulations in order to achieve a strong fundamental understanding of human subject research. This role is hospital based.

What you will do in this role:

• Supports enrolling patients onto clinical trials through recruitment, screening, enrollment and follow up of eligible subjects according to protocol requirements
• Responsible for working with the principal investigator to meet or exceed study enrollment.
• Reviews the study design and inclusion/exclusion criteria with physician and patient
• Ensures the protection of study patients by verifying informed consent procedures and adhering to protocol requirements/compliance
• Ensures the integrity of the data submitted on Case Report Forms or other data collection tools by careful source document review; monitors data for missing or implausible data
• Ensures that adequate and accurate records are maintained for inspecting
• Creates study specific tools for source documentation when not provided by sponsor
• Collects, completes, and enters data into study specific case report forms or electronic data capture systems
• Generates and tracks drug shipments, device shipments, and supplies as needed
• Reports and follows up on serious adverse events as necessary
• Implements study-specific communications
• Ensures timely adherence to protocol requirements
• Responsible for completion of all required documentation according to site works guidelines
• Ensures timely and accurate data completion
• Maintains accurate and complete records including regulatory documents when applicable, signed informed consent forms, source documentation, drug dispensing logs, device utilization logs, subject logs and study-related communications
• Tracks and reports adverse events, serious adverse events, protocol waivers, deviations, and violations
• Communicates all protocol-related issues to appropriate study colleagues or manager
• Attends study specific on site meetings, investigator meetings, conference calls and monthly CRC meetings as required or asked to do so
• Apprises principal investigator, Research Operations Director and Regional Site Manager of all study specific medical issues for guidance
• Assists sponsor and US FDA audit teams
• Reviews and responds to any monitoring and auditing findings and escalates issues defined by Regional Site Manager
• Maintains patient confidentiality according to ethical and legal requirements
• Assists in providing coverage for satellite clinic sites as necessary
• Responsible for coverage after hours and on weekends as necessary

What qualifications you will need:

• Associate’s Degree required, Bachelors Degree preferred.
• Active RN License required
• Knowledge of federal regulations, good clinical practices (GCP)
• Knowledge of medical and research terminology
• Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel
• Excellent Verbal and written communication skills
• Excellent interpersonal skills
• The ability to communicate and work effectively with a diverse team of professionals
• Organizational and prioritizing capabilities
• The ability to work independently in a fast pace environment with minimal supervision at off-site facilities

Benefits

Mission Health, offers a total rewards package that supports the health, life, career and retirement of our colleagues. The available plans and programs include:

• Comprehensive benefitsfor medical, prescription drug, dental, vision, behavioral health and telemedicine services
• Wellbeing support,including free counseling and referral services
• Time away from workprograms for paid time off, paid family leave, long- and short-term disability coverage and leaves of absence
• Savings and retirement resources, including a 401(k) Plan with a 100% match on 3% to 9% of pay (based on years of service), Employee Stock Purchase Plan, flexible spending accounts, preferred banking partnerships, retirement readiness tools, rollover support and financial wellbeing counseling
• Education supportthrough tuition assistance, student loan assistance, certification support, dependent scholarships and a partnership with Galen College of Nursing
• Additional benefitsfor fertility and family building, adoption assistance, life insurance, supplemental health protection plans, auto and home insurance, legal counseling, identity theft protection and consumer discounts

Learn more about Employee Benefits

Note: Eligibility for benefits may vary by location.

We are an equal opportunity employer. We do not discriminate on the basis of race, religion, color, national origin, gender, sexual orientation, age, marital status, veteran status, or disability status.