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Clinical Research Pre Screening Jobs in Raleigh, NC

Clinical Research Coordinator

Chapel Hill, NC · On-site

$22.25 - $29.50/hr

Conduct telephone and in-person interviews with participants, including screening for eligibility ... Critical Illness, Accident, and Hospital * 401(k) Retirement Plan - Pre-tax and Roth post-tax ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Screen, enroll, and monitor research participants while ensuring protocol adherence and participant ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Other tasks may include EMR review, participant screening, samples shipping, IP management, query ... Clinical Research-trials execution Other Requirements: * Necessary licenses, registrations ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

As a Clinical Research Coordinator in the Ophthalmology Clinical Research Unit (CRU) , you will ... Screen, recruit, consent, and retain study participants according to protocol requirements.

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

As a Clinical Research Coordinator in the Ophthalmology Clinical Research Unit (CRU) , you will ... Screen, recruit, consent, and retain study participants according to protocol requirements.

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Screens participants for greater than minimal risk or complex studies (e.g., procedural and ... Uses clinical research management system and its reports to manage research participants ...

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Screens participants for greater than minimal risk or complex studies (e.g., procedural and ... Uses clinical research management system and its reports to manage research participants ...

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Clinical Research Pre Screening information

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How much do clinical research pre screening jobs pay per hour?

As of Sep 5, 2026, the average hourly pay for clinical research pre screening in Raleigh, NC is $22.08, according to ZipRecruiter salary data. Most workers in this role earn between $16.83 and $25.24 per hour, depending on experience, location, and employer.

What is a clinical research pre screening specialist?

A Clinical Research Pre Screening specialist is responsible for evaluating potential participants to determine if they meet the basic eligibility criteria for clinical trials. They typically review medical histories, conduct initial assessments, and communicate with patients about the study requirements. This role is crucial in ensuring that only suitable candidates proceed to the next stages of the clinical trial process, which helps maintain the integrity and safety of the research. Pre screening specialists often work closely with clinical research coordinators and investigators.

What are the key skills and qualifications needed to thrive as a clinical research pre screening specialist?

To thrive as a Clinical Research Pre-Screening Specialist, you need a background in life sciences or healthcare, knowledge of research protocols, and attention to regulatory guidelines. Familiarity with clinical trial management systems (CTMS), electronic data capture (EDC) tools, and Good Clinical Practice (GCP) certification is often required. Strong interpersonal skills, attention to detail, and effective communication help in accurately evaluating candidates and collaborating with research teams. These skills ensure the accurate identification of eligible participants, compliance with study requirements, and smooth progression of clinical trials.

What are some common challenges faced by clinical research pre screening professionals, and how can they be addressed?

Clinical Research Pre-Screening professionals often face challenges such as accurately identifying eligible participants from large pools of applicants and ensuring strict adherence to study protocols and regulatory requirements. Managing sensitive patient data and maintaining clear communication with both clinical teams and potential participants can also be demanding. To address these challenges, it's important to stay organized, use standardized screening tools, and participate in regular training on compliance and privacy practices. Collaborating closely with research coordinators and maintaining up-to-date knowledge of study criteria can greatly improve efficiency and accuracy in pre-screening processes.

What is the difference between Clinical Research Pre Screening vs Clinical Research Coordinator?

AspectClinical Research Pre ScreeningClinical Research Coordinator
Primary RoleInitial participant eligibility assessment and screeningOversees entire study process, including recruitment, data collection, and follow-up
Required CredentialsHigh school diploma or equivalent; some roles may require clinical or research certificationsBachelor's degree in health or related field; often requires clinical research certification
Work EnvironmentScreening sites, clinics, or research facilitiesResearch sites, hospitals, clinics, or research institutions
Employer & Industry UsageUsed mainly during the participant recruitment phaseInvolved throughout the clinical trial lifecycle

While Clinical Research Pre Screening focuses on assessing participant eligibility at the start of a study, Clinical Research Coordinators manage the overall conduct of the trial, including recruitment, data collection, and compliance. Both roles are essential but differ in scope and responsibilities within the clinical research process.

What cities near Raleigh, NC are hiring for Clinical Research Pre Screening jobs?

Cities near Raleigh, NC with the most Clinical Research Pre Screening job openings:

Infographic showing various Clinical Research Pre Screening job openings in Raleigh, NC as of August 2026, with employment types broken down into 3% As Needed, 72% Full Time, 18% Part Time, and 7% Contract. Highlights an 95% Physical, 1% Hybrid, and 4% Remote job distribution, with an average salary of $45,922 per year, or $22.1 per hour.

Clinical Research Specialist, Senior - Duke Cancer Institute

Duke University

Durham, NC • On-site

Full-time

Medical, Dental, Retirement

Re-posted yesterday


Duke University rating

6.7

Company rating: 6.7 out of 10

Based on 55 frontline employees who took The Breakroom Quiz

491st of 630 rated colleges and universities


Job description

School of Medicine:
Established in 1930, Duke University School of Medicine is the youngest of the nation's top medical schools. Ranked sixth among medical schools in the nation, the School takes pride in being an inclusive community of outstanding learners, investigators, clinicians, and staff where interdisciplinary collaboration is embraced and great ideas accelerate translation of fundamental scientific discoveries to improve human health locally and around the globe. Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more than 6,200 staff, the Duke University School of Medicine along with the Duke University School of Nursing, and Duke University Health System comprise Duke Health, a world-class academic medical center. The Health System encompasses Duke University Hospital, Duke Regional Hospital, Duke Raleigh Hospital, Duke Health Integrated Practice, Duke Primary Care, Duke Home Care and Hospice, Duke Health and Wellness, and multiple affiliations.
Be You.
The Duke Cancer Institute's National Clinical Trials Network (NCTN) Clinical Research Program is seeking a Clinical Research Specialist, Senior to join the Oncology Clinical Research Unit (CRU). In this role, you will play a critical part in supporting cancer clinical trials that advance groundbreaking research and improve patient outcomes.
You will work closely with study teams to manage clinical research data, maintain study documentation, and ensure compliance with research protocols, regulatory requirements, and institutional standards. This position is ideal for a detail-oriented professional who enjoys working with data, collaborating with multidisciplinary teams, and contributing to innovative oncology research.
Minimum Requirements
  • Associate's degree.
  • One year of relevant experience.
  • Completion of the DOCR North Carolina State Approved Clinical Research Pre-Apprenticeship Program may substitute for the required experience.
  • Strong organizational and time management skills.
  • Critical thinking and problem-solving abilities.
  • Ability to accurately manage and document clinical research data.
  • Effective verbal and written communication skills.

Preferred Qualifications
  • Bachelor's degree strongly preferred.
  • Previous experience supporting clinical research studies or clinical trials.
  • Experience with Electronic Data Capture (EDC) systems and electronic Case Report Forms (eCRFs).
  • Familiarity with Good Clinical Practice (GCP), FDA regulations, and human subject protection requirements.
  • Experience working in oncology research or an academic medical center environment.
  • Demonstrated attention to detail and commitment to data quality.

Other Requirements
  • Maintain all Duke and protocol-specific training, certifications, and research compliance requirements.
  • Ability to handle and process biological research specimens according to protocol requirements.
  • Ability to work onsite in support of clinical research operations.

Be Bold.
As a Clinical Research Specialist, Senior, you will:
  • Manage clinical research data activities by entering, reviewing, validating, and maintaining study data within Electronic Data Capture systems while ensuring data accuracy, completeness, security, and regulatory compliance.
  • Complete and maintain study documentation including paper and electronic Case Report Forms (CRFs and eCRFs), source documentation, study files, participant records, and regulatory documents according to protocol and Standard Operating Procedures.
  • Support participant research activities by screening participants for eligible studies, facilitating consent activities for minimal-risk protocols, scheduling study visits, preparing study materials, and maintaining participant documentation.
  • Monitor and resolve data discrepancies by independently investigating incomplete, inaccurate, or missing information, coordinating with study teams, and implementing quality assurance procedures to maintain high-quality research data.
  • Process and manage research specimens by collecting, preparing, shipping, tracking, and maintaining specimen inventories in accordance with protocol requirements and laboratory standards.
  • Collaborate with multidisciplinary teams including investigators, clinical research staff, sponsors, and regulatory personnel to support protocol implementation, address routine study issues, and ensure successful trial execution.
  • Promote ethical research conduct by adhering to federal regulations, institutional policies, Good Clinical Practice guidelines, human subject protection standards, and research participant safety requirements.
  • Contribute to continuous improvement efforts by participating in team meetings, committees, educational opportunities, and collaborative initiatives that strengthen research operations and professional development.

Choose Duke.
The Duke Cancer Institute is one of the nation's leading cancer centers, bringing together world-class clinicians, researchers, and healthcare professionals committed to advancing cancer prevention, treatment, and survivorship. The Oncology Clinical Research Unit supports a robust portfolio of clinical trials that provide patients access to innovative therapies while helping shape the future of cancer care.
As part of the National Clinical Trials Network Clinical Research Program, you will work alongside dedicated professionals who are passionate about scientific discovery, collaboration, and excellence. This role offers the opportunity to contribute directly to research that impacts patients locally and globally while building your career within one of the country's premier academic health systems.
Job Code: 00000803 CLINICAL RESEARCH SPECIALIST, SR
Job Level: 50
Anticipated Pay Range: Duke University provides an annual base salary range for this position as USD $23.00 to USD $34.50. Duke University considers factors such as (but not limited to) scope and responsibilities of the position; candidate's work experience, education/training, and key skills; internal peer equity; as well as market and organizational considerations when extending an offer.
Your total compensation goes beyond the dollars on your paycheck. Duke provides comprehensive and competitive medical and dental care programs, generous retirement benefits, and a wide array of family-friendly and cultural programs to eligible team members. Learn more at: https://hr.duke.edu/benefits/
Equal Opportunity Employer: Duke is an Equal Opportunity Employer committed to providing employment opportunity without regard to an individual's age, color, disability, gender, gender expression, gender identity, genetic information, national origin, race, religion, sex (including pregnancy and pregnancy- related conditions), sexual orientation, or military status.
Duke aspires to create a community built on collaboration, innovation, creativity, and belonging. Our collective success depends on the robust exchange of ideas-an exchange that is best when the rich diversity of our perspectives, backgrounds, and experiences flourishes. To achieve this exchange, it is essential that all members of the community feel secure and welcome, that the contributions of all individuals are respected, and that all voices are heard. All members of our community have a responsibility to uphold these values.
Essential Physical Job Functions:
Certain jobs at Duke University and Duke University Health System may include essential job functions that require specific physical and/or mental abilities. Additional information and reasonable accommodation(s) can be requested with Duke Access and Accommodations Services (email: DAAS@duke.edu; phone: 919-668-1267).

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About Duke University

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Duke is regarded as one of America's leading research universities. Located in Durham, North Carolina, Duke is positioned in the heart of the Research Triangle, which is ranked annually as one of the best places in the country to work and live. Duke has more than 15,000 students who study and conduct research in its 10 undergraduate, graduate, and professional schools. With about 40,000 employees, Duke is the third largest private employer in North Carolina, and it now has international programs in more than 150 countries.

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Colleges, universities, and professional schools and hospitals

Company size

10,000+ Employees

Headquarters location

Durham, NC, US