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Research Operations Coordinator Jobs in Raleigh, NC

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

As the Clinical Research Coordinator, you will conduct clinical research studies, with a focus on ... Be Bold. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

As the Clinical Research Coordinator, you will conduct clinical research studies, with a focus on ... Be Bold. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more ... Be Bold. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Composed of more than 2,600 faculty physicians and researchers, nearly 2,000 students, and more ... Be Bold. Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more ... Operations: Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and ...

Duke University

Clinical Research Coordinator

Durham, NC · On-site

$23.50 - $31.25/hr

Composed of more than 2,500 faculty physicians and researchers, more than 1,300 students, and more ... Operations:Recognizes when typical agreements (MTAs, CDAs, DUAs, DTAs, etc.) are necessary and ...

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Research Operations Coordinator information

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$13

$24

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How much do research operations coordinator jobs pay per hour?

As of Sep 4, 2026, the average hourly pay for research operations coordinator in Raleigh, NC is $24.07, according to ZipRecruiter salary data. Most workers in this role earn between $19.18 and $27.12 per hour, depending on experience, location, and employer.

What is a research operations coordinator?

Research Operations Coordinators are professionals who support and streamline the administrative, logistical, and operational aspects of research projects within an organization. They manage research schedules, facilitate communication between teams, coordinate resources, and ensure compliance with institutional and regulatory requirements. Their goal is to help researchers focus on their core scientific work by handling the essential behind-the-scenes processes that keep projects running smoothly.

How does a research operations coordinator typically support collaboration between research teams and other departments?

A Research Operations Coordinator plays a key role in facilitating smooth communication and workflow between research teams and departments such as legal, finance, and IT. They help coordinate project timelines, manage documentation, and ensure compliance with institutional or regulatory guidelines. By organizing meetings, tracking project milestones, and addressing logistical needs, they enable researchers to focus on their core scientific work while ensuring all stakeholders remain aligned. This collaborative support is essential for the timely and effective execution of research projects.

What are the key skills and qualifications needed to thrive as a research operations coordinator, and why are they important?

To thrive as a Research Operations Coordinator, you need strong organizational abilities, project management experience, and a relevant bachelor's degree, often in a scientific or administrative field. Familiarity with research compliance systems, data management tools like Excel or REDCap, and certifications such as CITI training are commonly required. Excellent communication, problem-solving skills, and attention to detail help you coordinate teams and ensure smooth research operations. These skills and qualities are essential for maintaining regulatory compliance, supporting efficient research workflows, and facilitating collaboration across departments.

What is the difference between Research Operations Coordinator vs Research Analyst?

AspectResearch Operations CoordinatorResearch Analyst
CredentialsBachelor's degree in related field; experience in research supportBachelor's or master's in research, data analysis, or related field
Work EnvironmentSupports research teams, manages logistics, and coordinates resourcesAnalyzes data, prepares reports, and interprets research findings
Employer & Industry UsageUsed in research institutions, corporations, and universities for operational supportCommon in market research, academic, and policy analysis roles

The Research Operations Coordinator primarily manages research logistics and supports research teams, focusing on operational efficiency. In contrast, the Research Analyst analyzes data and interprets research results. Both roles require strong organizational skills, but their core responsibilities differ, with the Coordinator handling logistics and the Analyst focusing on data analysis.

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

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

What job categories do people searching Research Operations Coordinator jobs in Raleigh, NC look for?

The top searched job categories for Research Operations Coordinator jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Research Operations Coordinator jobs?

Cities near Raleigh, NC with the most Research Operations Coordinator job openings:

Research Operations Coordinator jobs near you
Infographic showing various Research Operations Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 81% Full Time, 15% Part Time, 1% Temporary, and 2% Contract. Highlights an 94% Physical, 2% Hybrid, and 4% Remote job distribution, with an average salary of $50,073 per year, or $24.1 per hour.

Clinical Research Coordinator - Durham, NC

Medix

Durham, NC • On-site

$27 - $30/hr

Full-time

Posted 25 days ago

Key responsibilities

  • Manage and conduct clinical trials from study startup through site closeout, including protocol implementation, vendor management, and subject recruitment.

  • Perform clinical procedures such as phlebotomy, IV/IM dose preparation and administration, fibroscans, ECGs, and vital signs, and collect and process laboratory specimens.

  • Ensure data integrity and regulatory compliance by applying ALCOA-C principles, preparing regulatory documentation, and monitoring adverse events.

Job description

Clinical Research Coordinator
Location: Onsite in Durham, NC
Schedule: Full-Time | Monday - Friday (Regular Schedule)
Employment Type: Contract
Position Overview
Medix is seeking a detail-oriented, highly skilled Clinical Research Coordinator (CRC) to manage and conduct clinical trials from study startup through site closeout.
Operating under Good Clinical Practice (GCP), ICH Guidelines, ALCOA-C principles, and organizational SOPs, this role combines end-to-end trial coordination, regulatory oversight, data integrity, project management, and direct patient care. The CRC serves as a central operational liaison between trial participants, site leadership, sponsors, CROs, vendors, and regulatory bodies.
Key Responsibilities
Clinical Trial Operations & Protocol Management
  • Implement and manage assigned protocols across the full study lifecycle, including study startup, vendor management, subject recruitment, protocol training, source development review, visit scheduling, and study closeout reporting.
  • Evaluate and prescreen potential study subjects via phone and in person; participate in the Informed Consent Form (ICF) process per protocol, local regulations, and IRB standards.
  • Develop, coordinate, and execute operational, research, and administrative strategies to manage assigned protocols effectively while incorporating key timelines, endpoints, vendors, and target patient populations.
  • Apply project management concepts to assess risk, elevate study quality, and align trial operations with organizational financial performance and stakeholder value.
  • Maintain a comprehensive understanding of the product development lifecycle, protocol design, critical data points, and disease processes under study.

Direct Patient Care & Clinical Procedures
  • Perform hands-on clinical duties within licensed scope, including phlebotomy (venipuncture and capillary puncture), intravenous/intramuscular (IV/IM) dose preparation and administration, fibroscans, ECGs, and vital signs.
  • Collect, process, package, and ship laboratory specimens in accordance with study protocols, local laws, and IATA regulations.
  • Promote respect for cultural diversity and conventions in all interactions with subjects, coworkers, and trial partners.

Regulatory Compliance & Data Integrity
  • Ensure strict data integrity by applying ALCOA-C principles when collecting, correcting, and transferring data into sponsor/CRO data capture systems and resolving EDC queries in a timely manner.
  • Prepare, collect, and submit regulatory documentation to Sponsors, CROs, and IRBs per GCP/ICH guidelines and Clinical Trial Agreements.
  • Monitor, document, and escalate Adverse Events (AEs), Serious Adverse Events (SAEs), Adverse Events of Special Interest (AESIs), and protocol deviations in accordance with protocols and Eximia SOPs.
  • Develop Quality Control (QC) strategies, communication/escalation workflows, and training tools to prepare for and participate in site audits and inspections.
  • Safeguard participant Protected Health Information (PHI) and protect confidential information across the study team.

Qualifications & Requirements
Education & Experience Options
  • Bachelor's Degree with 1+ years of experience as a Clinical Research Coordinator, OR
  • Associate Degree with 3+ years of experience as a Clinical Research Coordinator, OR
  • High School Diploma / Technical Degree with 5+ years of experience as a Clinical Research Coordinator.

Required Licenses & Certifications
  • Active Phlebotomy certification (where applicable and required by state law).
  • Intravenous (IV) / Intramuscular (IM) dose administration and preparation certification (where applicable and required by state law).
  • Certified Clinical Research Coordinator (CCRC) certification through ACRP or SOCRA (required within 6 months of employment).

Preferred Skills & Competencies
  • Domain Knowledge: Advanced knowledge of medical terminology, protocol design, and specimen processing standards.
  • Technical Skills: Proficient in clinical trial software/EDC systems, Microsoft Office Suite, and standard office hardware.
  • Operational Leadership: Proven ability to work independently, manage multiple deliverables, adapt to rapidly changing daily schedules, and develop team members.
  • Core Strengths: Excellent verbal, written, and interpersonal communication skills; highly organized, detail-oriented, and proficient in strategic problem-solving.

* We will consider for employment all qualified Applicants, including those with criminal histories, in a manner consistent with the requirements of applicable federal, state, and local laws, including the City of Los Angeles' Fair Chance Initiative for Hiring Ordinance (FCIHO), Los Angeles Fair Chance Ordinance for Employers (ULAC), The San Francisco Fair Chance Ordinance (FCO), and the California Fair Chance Act (CFCA).
* As a job position within our Clinical Sciences division, a successful completion of a background check may be required as a condition of employment. This requirement is directly related to essential job functions including but not limited to: high-risk working environments (laboratories, clinical settings), handling hazards chemicals or lab specimens, conducting direct patient care, accessing medical and confidential records, access to prescription medication or other drugs, and job duties that can cause serious injury or death as a result of error. Due to these job duties, this position has a significant impact on the business operations and reputation, as well as the safety and well-being of individuals who may be cared for as part of the job position or who may interact with staff or clients.
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About Medix Staffing Solutions

Sourced by ZipRecruiter

Since 2001, we’ve been dedicated to helping you achieve your goals. Medix was created to become a leading provider of workforce solutions for clients and candidates across the healthcare and life sciences industries. Today, we are that leader. Headquartered in Chicago, we have 23 offices across the United States, and staff talent around the world. Medix is committed to fulfilling our core purpose as an organization: to positively impact the lives of our talent, clients, and teammates through employment, philanthropy, and opportunity. The combination of purpose and values has nurtured our thriving culture that encourages our internal team to excel at work and in everyday life.

Industry

Recruiting and staffing services

Company size

1,001 - 5,000 Employees

Headquarters location

Chicago, IL, US

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