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Full Time Clinical Research Monitor Jobs in Raleigh, NC

UNC-Chapel Hill

Clinical Research Assistant

Chapel Hill, NC · On-site

$19 - $21/hr

... Full-time/Part-time Full-Time Temporary Hours per week 40 Work Schedule Monday - Friday, 8:00 AM ... monitor visits. Additionally, the Clinical Research Assistant will track subject visits and site ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Lead study monitoring, audit preparation, and corrective action activities. * Support study startup ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

Clinical Research Coordinator - Neurosurgery Research Be You. At Duke, we celebrate individuality ... Lead study monitoring, audit preparation, and corrective action activities. * Support study startup ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

As a Clinical Research Coordinator in the Ophthalmology Clinical Research Unit (CRU) , you will ... Support study monitoring visits, audits, inspections, and sponsor reviews. * Address findings and ...

Duke University

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 ... Support study monitoring visits, audits, inspections, and sponsor reviews. * Address findings and ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

This full-time onsite Clinical Research Professional (CRP) will participate in research conducted ... May train others. Prepares for and provides support for study monitoring and audit visits ...

Parexel

Senior Clinical Research Associate

Raleigh, NC · On-site +1

Hours: Full Time / 40 hours per week Summary of Duties: Engaged in monitoring clinical research that involves understanding human diseases and improving human health. Monitor and oversee clinical ...

Duke University

Clinical Research Coordinator

Durham, NC

$23.50 - $31.25/hr

May train others. Prepares for and provides support for study monitoring and audit visits ... Uses clinical research management system and its reports to manage research participants ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

May train others. Prepares for and provides support for study monitoring and audit visits ... Uses clinical research management system and its reports to manage research participants ...

Care Access

Clinical Research Coordinator I

Raleigh, NC · On-site

$55K - $85K/yr

Coordinate and attend pre-study site visits, site initiation visits, and monitor visits with ... Benefits & Perks (US Full Time Employees) * Paid Time Off (PTO) and Company Paid Holidays * 100 ...

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Full Time Clinical Research Monitor information

What is a full time clinical research monitor?

Full Time Clinical Research Monitors, also known as Clinical Research Associates (CRAs), are professionals responsible for overseeing clinical trials to ensure they are conducted according to regulatory requirements, ethical standards, and study protocols. They visit research sites to review data, verify patient records, and ensure participant safety. Their work helps confirm the accuracy and integrity of clinical trial results, playing a critical role in the development of new medical treatments and drugs.

What are the key skills and qualifications needed to thrive as a full time clinical research monitor?

To thrive as a Full Time Clinical Research Monitor, you need a solid understanding of clinical trial protocols, Good Clinical Practice (GCP) guidelines, and a background in life sciences or nursing, often supported by a bachelor's degree. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and sometimes certification such as ACRP or SOCRA is highly valuable. Outstanding attention to detail, strong organizational skills, and effective communication are crucial soft skills for ensuring compliance and fostering collaboration among research teams. These competencies are critical for maintaining data integrity, patient safety, and regulatory compliance throughout the clinical trial process.

What are some common challenges full time clinical research monitors face when overseeing multiple clinical trial sites?

Full Time Clinical Research Monitors often encounter challenges such as coordinating communication across multiple sites, managing diverse site staff, and ensuring consistent adherence to protocols and regulatory requirements. Balancing travel, documentation, and follow-up visits can be demanding, especially when sites are geographically dispersed. Strong organizational skills, attention to detail, and effective relationship-building are crucial to ensuring trials progress smoothly and data integrity is maintained.

What are the most commonly searched types of Clinical Research Monitor jobs in Raleigh, NC?

The most popular types of Clinical Research Monitor jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Full Time Clinical Research Monitor jobs?

Cities near Raleigh, NC with the most Full Time Clinical Research Monitor job openings:

Full Time Clinical Research Monitor jobs near you
Infographic showing various Full Time Clinical Research Monitor job openings in Raleigh, NC as of August 2026, with employment types broken down into 100% Full Time. Highlights an 79% In-person, and 21% Remote job distribution.

Clinical Research Coordinator

Cary, NC • On-site

Revival Research Institute, LLC
See more jobs at Revival Research Institute, LLCexternal

$22.50 - $30/hr

Full-time

Re-posted 7 days ago

Job description

About Revival Research Institute
Revival Research Institute, LLC has been conducting industry-sponsored clinical trials since 2015. Headquartered in Metro Detroit, we operate sites across Michigan, Texas, Illinois, New Jersey, and North Carolina, and have been recognized nationally for the quality of the data we deliver to our sponsors. 
About This Role
This is not an entry-level position. We are hiring an experienced site-based coordinator who has independently run industry-sponsored interventional trials and can take ownership of assigned protocols from site initiation visit through close-out.
Clinical Research Coordinators at Revival coordinate and manage multiple concurrent studies and support the Investigators and clinical staff with study-related tasks including, but not limited to:
Responsibilities
  1. Screening, recruitment, and enrollment. Pre-screen candidates against inclusion/exclusion criteria, independently obtain informed consent on interventional protocols in accordance with ICH-GCP and 21 CFR Part 50, and conduct study visits per protocol. Collect, process, and ship research specimens, including IATA-regulated shipments, where applicable.
  2. Data and monitoring. Obtain, review, and maintain source documents contemporaneously. Enter data into EDC within sponsor-specified timelines and resolve queries within guidelines provided in the protocol. Host monitoring visits, and drive CRA findings and follow-up letters through to resolution.
  3. Regulatory and quality. Own the organization and completeness of all trial-related documents and correspondence across regulatory binders and eRegulatory systems. Implement and maintain quality control and assurance methods at the study level, and maintain inspection-ready files at all times.
  4. Sponsor and IRB communication. Serve as day-to-day point of contact for sponsors, CRAs, central labs, and IRT/IWRS vendors. Independently prepare and submit regulatory documents including amendments, continuing reviews, adverse and serious adverse event reports within required reporting windows, and protocol deviation reports.
  5. Investigational product accountability. Manage IP receipt, dispensing, reconciliation, storage conditions, and temperature excursion documentation in accordance with the protocol and sponsor requirements.
  6. Professional and technical knowledge. Maintain current working knowledge of ICH-GCP E6(R3), applicable FDA regulations, and evolving sponsor and site practices. Maintain certification and required training.
  7. Participant communication and confidentiality. Communicate with research participants and their families throughout the study lifecycle, support retention across visit schedules, and protect participant confidentiality in accordance with HIPAA.
Required Qualifications
  1. 2+ years as a Clinical Research Coordinator at a research site, serving as primary coordinator on industry-sponsored interventional trials. Academic-only, registry-only, or observational/minimal-risk experience does not meet this requirement.
  2. Demonstrated experience independently obtaining informed consent on interventional protocols.
  3. Hands-on experience with EDC platforms.
  4. Demonstrated experience hosting monitoring visits and resolving monitoring findings independently.
  5. Working knowledge of ICH-GCP E6(R3) and 21 CFR Parts 11, 50, 54, 56, and 312, and HIPAA.
  6. Current phlebotomy competency, as well as IV certification, is preferred.
  7. Proficiency in conducting physical assessments, including comfort with vital signs and 12-lead ECG acquisition.
  8. Master's degree in a health-related field, or equivalent clinical research site experience.
  9. Strong computer proficiency including Microsoft Office (Word, Excel, Outlook); excellent verbal and written communication; ability to work independently, manage competing protocol deadlines, and assume ownership of assigned studies.
  10. Ability to work on-site in Cary, NC.

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