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Full Time Human Subject Research Jobs in Raleigh, NC

... subject enrollment, human protection, and expeditious delivery of accurate evaluable data. Due to our continued growth, we are hiring for a Clinical Research Coordinator II at Wake Research, an M3 ...

Clinical Research Coordinator II (On-site)

Raleigh, NC · On-site

$23.50 - $31.25/hr

... subject enrollment, human protection, and expeditious delivery of accurate evaluable data. Due to our continued growth, we are hiring for a Clinical Research Coordinator II at Wake Research, an M3 ...

About the Role The Carolina Federation is seeking a full-time HR and Operations Director to oversee ... Work with the COO to research, develop, implement, and continuously refine organizational policies ...

New

... ID S027344 Full-time/Part-time Full-Time Temporary Hours per week 40 Work Schedule Position ... The techniques likely to be used include human endothelial cell culture, dissection of mouse ...

Research Technician

Chapel Hill, NC · On-site

$30 - $31/hr

... Full-Time Temporary Hours per week 40 Work Schedule Monday - Friday, 8:30 AM - 5:00 PM Position ... The Office of Human Resources will not be able to provide specific updates regarding position or ...

Research Assistant

Chapel Hill, NC · On-site

$15 - $15.63/hr

... Full-Time Temporary Hours per week 40 Work Schedule Monday - Friday, 9:00 AM - 5:00 PM Position ... The Office of Human Resources will not be able to provide specific updates regarding position or ...

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Full Time Human Subject Research information

What are the key skills and qualifications needed to thrive in Full Time Human Subject Research, and why are they important?

To thrive in Full Time Human Subject Research, you need a solid background in scientific methodology, ethical research practices, and often a degree in a relevant field such as psychology, biology, or public health. Familiarity with data collection tools, statistical software (like SPSS or R), and Institutional Review Board (IRB) protocols is typically required. Exceptional attention to detail, strong interpersonal skills, and clear communication help ensure accurate data collection and ethical participant interactions. These skills and qualities are crucial for producing valid research outcomes while safeguarding participant rights and well-being.

What are the typical challenges faced by professionals in full-time human subject research roles?

Professionals working in full-time human subject research often face challenges such as recruiting and retaining participants, ensuring strict compliance with ethical guidelines and institutional review board (IRB) protocols, and managing sensitive data securely. Balancing administrative tasks with hands-on research activities can also be demanding, as can coordinating with multidisciplinary teams including clinicians, statisticians, and regulatory staff. Strong organizational skills and adaptability are key to successfully navigating these complexities while maintaining the integrity of the study.

What is a Full Time Human Subject Researcher?

A Full Time Human Subject Researcher is a professional who conducts scientific studies involving human participants. Their work typically includes designing research protocols, recruiting and monitoring subjects, collecting data, and ensuring all research is conducted ethically and in compliance with regulations. They may work in academic, clinical, or private research settings and often collaborate with other scientists and medical professionals. The goal is to advance knowledge in fields such as medicine, psychology, or public health, while prioritizing the safety and rights of human subjects.

What is the difference between Full Time Human Subject Research vs Full Time Clinical Research Coordinator?

AspectFull Time Human Subject ResearchFull Time Clinical Research Coordinator
CredentialsOften requires a bachelor's degree in health sciences, psychology, or related fields; certifications like CITI are commonTypically requires a bachelor's degree; certifications like CITI or CCRP are advantageous
Work EnvironmentResearch institutions, universities, hospitals conducting human subject studiesClinical trial sites, hospitals, research centers managing patient studies
Employer & IndustryAcademic, government, or private research organizationsPharmaceutical companies, hospitals, clinical research organizations

Both roles involve working with human subjects in research settings, but Full Time Human Subject Research often focuses on designing and analyzing studies, while Clinical Research Coordinators manage day-to-day trial operations. Understanding these differences helps job seekers identify the right career path in clinical research.

What are the most commonly searched types of Human Subject Research jobs in Raleigh, NC? The most popular types of Human Subject Research jobs in Raleigh, NC are:
What are popular job titles related to Full Time Human Subject Research jobs in Raleigh, NC? For Full Time Human Subject Research jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Full Time Human Subject Research jobs in Raleigh, NC look for? The top searched job categories for Full Time Human Subject Research jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Full Time Human Subject Research jobs? Cities near Raleigh, NC with the most Full Time Human Subject Research job openings:
Infographic showing various Full Time Human Subject Research job openings in Raleigh, NC as of May 2026, with employment types broken down into 57% Full Time, 29% Part Time, and 14% Temporary. Highlights an 93% In-person, and 7% Hybrid job distribution.
Clinical Studies RN II, Surgery Trauma

Clinical Studies RN II, Surgery Trauma

Advocate Aurora Health

Wake Forest, NC • On-site

$38.20 - $57.30/hr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 22 days ago


Advocate Aurora Health rating

7.6

Company rating: 7.6 out of 10

Based on 761 frontline employees who took The Breakroom Quiz

181st of 864 rated healthcare providers


Job description

Department:
36205 Wake Forest University Health Sciences - Surgery: Trauma
Status:
Full time
Benefits Eligible:
Yes
Hours Per Week:
40
Schedule Details/Additional Information:
varies
Pay Range
$38.20 - $57.30
JOB SUMMARY
The Clinical Research Nurse II provides protocol driven nursing treatment to a specific group of patients who are participating in clinical research studies within the Trauma Surgery department of Atrium Health Wake Forest Baptist. They function as part of a research team that may consist of Investigators, Clinical Studies Coordinators, Data Managers, Regulatory Coordinators, and other Staff. Under the direction of the Investigator, the Clinical Research Nurse II is responsible for subject recruitment, eligibility, enrollment, informed consent, subject retention, education, and protocol adherence. Clinical responsibilities include ensuring the protocol is conducted in a high-quality manner in compliance with Clinical Protocol and Data management (CPDM) unit, State, and Federal guidelines. In addition, communicates research-related information to patients, families, nursing, and medical staff as necessary. Cross trains to support the other Clinical Studies Nurses when needed.
EDUCATION/EXPERIENCE
An associate's degree in Nursing from an accredited School of Nursing with one year of nursing experience preferably in a related field such as research, acute care, or a specialty area is required.
A Bachelor's degree in Nursing with two or more years of nursing experience is preferred.
LICENSURE, CERTIFICATION, and/or REGISTRATION
  • Licensure as a Registered Nurse (RN) in the State of North Carolina required.
  • Must complete the CITI certification for Human Subject Research if not already completed and any additional required training for research coordinators.

ESSENTIAL FUNCTIONS
Works under the direction and supervision of Dr. James Holmes IV and the Study Investigators. Also receives supervision and mentoring from the Study Team.
Knowledge and understanding of policies, procedures, and regulations governing human subject's research and incorporates them in the conduct of research and care of participants.
Actively screens Burn and Trauma patients for eligibility.
Actively carries out Study protocol interventions (which may include ultrasound, administering study medication, drawing blood, responding to Level 1 Trauma Codes, familiarity with Operating Room protocol, coordinating study visits and procedures, etc.).
Coordinates patient schedules and provides information for a successful visit to meet the required protocol procedures, data collection time points and nursing care.
Interacts with critically ill Trauma and Burn victims and their families.
Coordinates with the physician and clinic staff to assure that all protocol requirements are scheduled and ordered.
Reviews Electronic Medical Record to ensure protocol compliance and appropriate data collection.
Assesses and enter the initial adverse event report and serious adverse events into the eIRB system e.
Follows-up with the assigned regulatory contact to resolve any outstanding reporting requirements in a prompt and appropriate manner
Attends relevant investigational and professional meetings to keep abreast of current developments in the field.
Serves as an advocate for human subjects by establishing and maintaining communication with Investigators, research staff, Sponsors, participants and others.
Performs other related duties incidental to the work described herein.
SKILLS/QUALIFICATIONS
  • Good communication skills
  • Ability to
  • Ability to provide indirect patient care
  • EPIC/ Encompass proficiency to include appropriate documentation of research notes
  • Basic computer skills

WORK ENVIRONMENT
  • Variable paced work schedule driven by protocol windows
  • Professionalism and communication skills being a must at all times
  • Occasionally subject to irregular hours

Our Commitment to You:
Advocate Health offers a comprehensive suite of Total Rewards: benefits and well-being programs, competitive compensation, generous retirement offerings, programs that invest in your career development and so much more - so you can live fully at and away from work, including:
Compensation
  • Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
  • Premium pay such as shift, on call, and more based on a teammate's job
  • Incentive pay for select positions
  • Opportunity for annual increases based on performance

Benefits and more
  • Paid Time Off programs
  • Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
  • Flexible Spending Accounts for eligible health care and dependent care expenses
  • Family benefits such as adoption assistance and paid parental leave
  • Defined contribution retirement plans with employer match and other financial wellness programs
  • Educational Assistance Program

About Advocate Health
Advocate Health is the third-largest nonprofit, integrated health system in the United States, created from the combination of Advocate Aurora Health and Atrium Health. Providing care under the names Advocate Health Care in Illinois; Atrium Health in the Carolinas, Georgia and Alabama; and Aurora Health Care in Wisconsin, Advocate Health is a national leader in clinical innovation, health outcomes, consumer experience and value-based care. Headquartered in Charlotte, North Carolina, Advocate Health services nearly 6 million patients and is engaged in hundreds of clinical trials and research studies, with Wake Forest University School of Medicine serving as the academic core of the enterprise. It is nationally recognized for its expertise in cardiology, neurosciences, oncology, pediatrics and rehabilitation, as well as organ transplants, burn treatments and specialized musculoskeletal programs. Advocate Health employs 155,000 teammates across 69 hospitals and over 1,000 care locations, and offers one of the nation's largest graduate medical education programs with over 2,000 residents and fellows across more than 200 programs. Committed to providing equitable care for all, Advocate Health provides more than $6 billion in annual community benefits.

What Advocate Aurora Health employees say

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About Advocate Healthcare

Sourced by ZipRecruiter

Advocate Healthcare, based in Oak Lawn, Illinois, United States, is a leading figure in the health care industry. Accessible via their official website, 'advocatehealth.com', this organization provides a wide variety of medical services and treatment options. Founded in 1995 through a merger of Evangelical Health Systems Corporation and Lutheran General HealthSystem, Advocate Healthcare has grown exponentially over the years. Now, it operates more than 400 sites of care, including 12 hospitals that encompass 11 acute care hospitals, the state’s largest integrated children’s network, five Level I trauma centers, and three Level II trauma centers. Upholding their values of equality, compassion, excellence, partnership and stewardship, Advocate Healthcare's mission is centered on building lifelong relationships with patients by delivering the best health outcomes and highest level of service through an integrated approach to care and wellness.

Industry

Hospitals and health care and social assistance

Company size

10,000+ Employees

Headquarters location

Oak Lawn, IL, US