
Clinical Research Coordinator Public Health Sciences
Winston-Salem, NCFull-time$26.55–39.85/hrPosted 1w agoStill listed 5 days ago
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At a glance
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Requirements
Credentials this posting asks for.
Job overview
The Clinical Research Coordinator supports Alzheimer’s disease research studies, particularly genetics research, through community outreach, participant recruitment, enrollment, and follow-up. Working with the Principal Investigator, Program Manager, research staff, and collaborating sites, the coordinator conducts participant visits, obtains consent, collects samples and assessments, and supports study documentation, regulatory compliance, and IRB submissions. The role includes travel to participant locations and may require occasional non-traditional hours.
Skills & qualifications
Skills
Qualifications
Benefits
Full job description
Department:
85043 Wake Forest University Health Sciences - Academic Public Health Sciences: Social Sciences
Status:
Full time
Benefits Eligible:
Yes
Hours Per Week:
40
Schedule Details/Additional Information:
M-F 8:30-5:30 and flexible hours
Ideal candidate has: A Bachelor's degree in public health, Basic Science, or a relevant clinical discipline, but a master’s degree is preferred. Experience in a medical and/or research setting. Paramedical or other clinical experience. One year of clinical and or survey research experience including interviewing, and supervision of data collection procedures. An equivalent combination of education and experience will be considered.
Phlebotomy license preferred Registered Record Administrator preferred Valid NC Driver's License
Pay Range: $26.55 - $39.85
The Clinical Research Coordinator supports Alzheimer’s disease (AD) research studies through community outreach, participant recruitment, enrollment, and follow-up. Working closely with the Principal Investigator, Program Manager, research staff, and collaborating sites, this position helps recruit participants for Alzheimer’s disease genetics research. Key responsibilities include conducting participant visits in community and residential settings, obtaining informed consent, collecting blood samples, administering cognitive assessments, and gathering family and medical histories. The coordinator also prepares and ships research specimens, participates in clinical classification meetings, and supports Institutional Review Board (IRB) submissions, regulatory compliance, and study documentation. This role requires strong judgment, organization, and communication skills, as well as the ability to travel to participant locations. Occasional non-traditional work hours may be required.
EDUCATION/EXPERIENCE
- Bachelor's degree with two years; experience in clinical research; or an equivalent combination of experience and education.
LICENSURE, CERTIFICATION, and/or REGISTRATION
- SOCRA or ACRP Certification preferred.
- Must complete the CITI certification for Human Subject Research if not already completed.
- All additional required WakeOne training for research coordinators.
ESSENTIAL FUNCTIONS
- Assists in the administration and coordination of all phases of the assigned project as directed.
- Responsible for ensuring that all aspects of the study are conducted following the study protocol.
- Represents the project by serving as the study liaison and representative.
- May guide other study personnel by providing training, direction, guidance, and evaluation of work activities.
- Coordinates and participates in recruitment data collection, and follow-up activities.
- Collect blood samples.
- Must be able to travel to collaborating institutions and travel to homes of the participants local, state, and nationally.
- Assists with the development of collection methods; creates and revises study materials, forms, manuals, and brochures as requested.
- Assists with and provides reports as requested.
- Provides guidance and/or performs data processing and coordinates data analysis; oversees quality assurance of data.
- Orders and maintains adequate supplies for the project.
- Initiate introductory visit following timeliness guidelines per study standards.
- Actively participates in outreach/community education and/or early detection/screening events around AD.
- Provide presentations around AD and other related dementias.
- Performs other related duties incidental to the work described herein
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
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Base compensation listed within the listed pay range based on factors such as qualifications, skills, relevant experience, and/or training
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Premium pay such as shift, on call, and more based on a teammate's job
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Incentive pay for select positions
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Opportunity for annual increases based on performance
Benefits and more
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Paid Time Off programs
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Health and welfare benefits such as medical, dental, vision, life, and Short- and Long-Term Disability
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Flexible Spending Accounts for eligible health care and dependent care expenses
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Family benefits such as adoption assistance and paid parental leave
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Defined contribution retirement plans with employer match and other financial wellness programs
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Educational Assistance Program
Note: Eligibility for programs listed above may depend on your FTE or status (e.g., full-time, part-time, per diem, temporary, etc.); please ask a Recruiter for more information during an interview.
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.
How this job compares
Set against the 604 open Clinical Research Coordinator jobs on Olive Jobs, counted November 4, 2026.
- Pay
- This posting$26.55–39.85/hr
- US median$24–35/hr178 hourly ranges
This range's midpoint, $33.20/hr, is 13% above the US median midpoint ($30/hr) — in the middle half of Clinical Research Coordinator hourly ranges across the US.
- Openings
- Olive Jobs lists 10 open Clinical Research Coordinator jobs in North Carolina and 604 across the US. 2% of them nationwide are listed as remote or flexible.
- Hiring the most across the US
- Mount Sinai Health System45 open
- Iterative Health39 open
- University of Miami39 open
- Experience
- This posting asks for at least 2 years of experience; Clinical Research Coordinator postings that state a minimum ask for 2 years at the median (397 postings).
- Education
- 191 of the 604 open Clinical Research Coordinator jobs (32%) ask for a bachelor's degree or higher.
Counted across the open, public US postings on Olive Jobs on November 4, 2026. Pay medians are the middle values of the low ends and of the high ends of postings that list both ends of a range in the same cadence (a yearly salary or an hourly rate); a range's midpoint is halfway between its ends. Pay and experience figures resting on fewer than 20 postings are left out.
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