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Clinical Data Coordinator Jobs in Raleigh, NC (NOW HIRING)

Job Overview The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...

Job Overview The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...

Job Overview The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant ...

Clinical Data Manager

Durham, NC · On-site

$68K - $171K/yr

Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s). * Perform data review and discrepancy resolution, as needed.

Clinical Data Manager

Durham, NC · On-site

$68K - $171K/yr

Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s). * Perform data review and discrepancy resolution, as needed.

Clinical Data Manager

Durham, NC · On-site

$68K - $171K/yr

Responsible for providing data review training and guidance to Sr. Clinical Data Coordinators that are supporting their trial(s). * Perform data review and discrepancy resolution, as needed.

Coordinates the receipt and inventory of all data related information, from clinical sites and vendors as appropriate to meet timelines for deliverables. Ensure all appropriate documentation and ...

Clinical Research Coordinator (CRC) - Raleigh, NC Location: Raleigh, NC Work Setup: On-site ... Accurately collect, review, and enter study data into Electronic Data Capture (EDC) systems.

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to ...

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to ...

The Contract Clinical Study Manager provides operational leadership, coordination, and oversight ... forms, data management plans, data transfer plans, and clinical data review activities ...

Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ... Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to ...

Coordinate with internal project team members, CROs, vendors, investigators, and study coordinators ... Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to ...

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Clinical Data Coordinator information

See Raleigh, NC salary details

$15

$28

$55

How much do clinical data coordinator jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for clinical data coordinator in Raleigh, NC is $28.82, according to ZipRecruiter salary data. Most workers in this role earn between $22.21 and $32.93 per hour, depending on experience, location, and employer.

What does a clinical data coordinator do?

A Clinical Data Coordinator is responsible for collecting, managing, and ensuring the quality of data generated from clinical trials and medical research studies. They work closely with clinical research teams to input, verify, and monitor data accuracy, integrity, and compliance with regulatory standards. Their work is vital for the successful analysis of clinical trial outcomes and for supporting the development of new medical treatments.

What does a clinical data coordinator do?

A clinical data coordinator is responsible for overseeing a number of data related tasks associated with running a clinical facility. In this career, your job duties include creating reports on patient data, developing programs that support a clinical study, and providing information to ensure regulatory compliance on behalf of the clinic. The qualifications needed to have a career as a clinical data coordinator include a bachelor's degree in computer science or a related field. You also need strong analytical skills and experience working with databases.

How does a clinical data coordinator typically collaborate with other teams during a clinical trial?

Clinical Data Coordinators work closely with clinical research associates, data managers, and regulatory teams to ensure the accurate collection and management of trial data. They frequently communicate with site staff to resolve data discrepancies and ensure adherence to protocol and data quality standards. Regular meetings and updates are common to address ongoing data queries, share progress, and align on timelines. This cross-functional collaboration is vital for maintaining the integrity of clinical trial data and supporting successful study outcomes.

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

To thrive as a Clinical Data Coordinator, you need strong analytical skills, attention to detail, and a background in life sciences or a related field, often supported by a bachelor’s degree. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools, and knowledge of regulatory standards such as GCP and FDA guidelines are essential. Excellent organizational skills, effective communication, and the ability to collaborate with multidisciplinary teams help set top candidates apart. These competencies ensure accurate data collection and integrity, which are crucial for the success and compliance of clinical trials.

What is the difference between Clinical Data Coordinator vs Clinical Research Associate?

AspectClinical Data CoordinatorClinical Research Associate
Primary RoleManage and ensure accuracy of clinical data collection and entryOversee clinical trial sites, monitor study progress, and ensure compliance
Required CredentialsTypically a bachelor's degree in health, life sciences, or related fieldUsually a bachelor's degree in health sciences, along with monitoring certifications
Work EnvironmentData management teams, clinical trial databases, research organizationsClinical sites, monitoring visits, regulatory agencies
Industry UsageCommon in clinical data management and research organizationsCommon in pharmaceutical companies and contract research organizations

The Clinical Data Coordinator focuses on managing and verifying clinical data accuracy, while the Clinical Research Associate monitors trial sites and ensures compliance. Both roles are essential in clinical research but differ in daily responsibilities and focus areas.

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

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

What are popular job titles related to Clinical Data Coordinator jobs in Raleigh, NC?

For Clinical Data Coordinator jobs in Raleigh, NC, the most frequently searched job titles are:

What job categories do people searching Clinical Data Coordinator jobs in Raleigh, NC look for?

The top searched job categories for Clinical Data Coordinator jobs in Raleigh, NC are:

What cities near Raleigh, NC are hiring for Clinical Data Coordinator jobs?

Cities near Raleigh, NC with the most Clinical Data Coordinator job openings:

Infographic showing various Clinical Data Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 2% As Needed, 81% Full Time, 5% Part Time, and 12% Contract. Highlights an 78% In-person, 10% Hybrid, and 12% Remote job distribution, with an average salary of $59,945 per year, or $28.8 per hour.

Senior Clinical Data Coordinator

IQVIA

Durham, NC • On-site

$50K - $126K/yr

Full-time

Posted 8 days ago


IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

63rd of 225 rated it services


Job description

Job Overview

The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of Phase I-IlI clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines to ensure that a quality work product is produced and timelines and deliverables are met.

Summary of the Essential Functions of the Job

  • Perform ongoing data review, including reconciliation of third party data streams and serious adverse event reconciliation with the safety database.
  • Perform User Acceptance Testing (UAT) of clinical databases.
  • Perform Quality Control (QC) of clinical databases.
  • Perform ongoing updates of Data Management-related documentation, as needed.

Minimum Requirements

  • Bachelor's degree OR certification in a related allied health profession from an appropriately accredited institution (i.e. RN, MT, PA, RT) is preferred, but individuals with commensurate experience will be considered.
  • Minimum of 3 years of data management experience is required.
  • Experience with Electronic Data Capture (EDC) system(s) is required.
  • Experience with Oracle Inc.'s Inform EDC system is preferred.
  • Oncology and/or inflammatory therapeutic area experience is preferred.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more athttps://jobs.iqvia.com

IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe

IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.

The potential base pay range for this role, when annualized, is $50,600.00 - $126,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

What IQVIA employees say

Pay

Benefits

Hours and flexibility

Workplace

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US