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

Fortrea

Senior Clinical Data Manager

Durham, NC · On-site

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 ...

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

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.

Belcan

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 ...

Belcan

Clinical Study Manager

Durham, NC

$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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

System One

Clinical Study Manager

Durham, NC · On-site

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 ...

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 ... Data Management & Quality Assurance * Collect, enter, review, and maintain research data with a ...

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Clinical Data Coordinator information

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How much do clinical data coordinator jobs pay per hour?

As of Aug 28, 2026, the average hourly pay for clinical data coordinator in Raleigh, NC is $26.18, according to ZipRecruiter salary data. Most workers in this role earn between $20.14 and $29.90 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.

More about Clinical Data Coordinator jobs

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:

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

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

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

Clinical Data Coordinator jobs near you
Infographic showing various Clinical Data Coordinator job openings in Raleigh, NC as of August 2026, with employment types broken down into 9% As Needed, 73% Full Time, 9% Part Time, and 9% Contract. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $54,446 per year, or $26.2 per hour.

Principal Clinical Data Manager

Raleigh, NC • On-site, Remote

Biodata Partners, Inc.
See more jobs at Biodata Partners, Inc.external

Contractor

Re-posted 7 days ago

Job description

 Job Summary:
Manage end-to-end delivery of data management services concurrently for single/multi-service projects with little-to-no guidance, ensuring quality deliverables on time and within budget to customer satisfaction. Provide comprehensive data management expertise to Clinical Data Management (CDM) team to provide high quality data management products that meet customer needs. Provide leadership to the team in the areas of project planning, execution, and close-out, communications and milestone deliverables. Perform a leadership role in specific CDM tasks (e.g. Subject Matter Expert (SME)). Comply with Good Clinical Practices (GCPs), applicable regulatory guidelines, SOPs, policies, and, where available, CDM guidance documents.
Responsibilities:
  • Effectively plan and execute multiple Data Management projects simultaneously. Provide updates directly to senior stakeholders as requested by line management.
  • Collaborate with Sponsor and stakeholders to develop effective project plans to include scope, goals, deliverables, required resources, risks, issues and milestone timing.
  • Assign tasks and responsibilities within Data Management to team members, in a manner that: optimizes team capability; delivers timely and accurate results; and supports the needs of the business.
  • Ensure that assigned team executes Data Management functions in accordance with CRO and/or Sponsor Standard Operating Procedures (SOPs).
  • Provide guidance to less-experienced Data Management staff.
  • Assess ongoing and future project resource needs on an ongoing basis with feedback to Line Management.
  • Triage and resolve issues throughout project lifecycle.
  • Ensure that project team members' performance supports project budget and delivery requirements.
  • Effectively manage project scope by ensuring any changes to scope are documented and approved through appropriate change management processes.
  • Participate in and/or contribute to Sponsor and/or Regulatory audits/inspections.
  • Attend regular meetings with the sponsor and/or project team, for discussions relating to data management issues and provides status updates for the project.
  • Track and report quality and performance metrics and KPIs as needed.
  • Active participation in the organization and department of both in-house and external training courses.
  • Adherence to SOPs as well as current ICH-GCP guidelines and other applicable standards demanded by the Regulatory Authorities.
  • Coordinate and manage training for Investigators, Data Coordinators and CRAs on the selected Data Systems for Data Processing.
  • Ensure quality of data in accordance with DM control documents for accuracy, completeness, consistency and validity, generate and submit queries as necessary to investigation sites, as well as the project team at large.
  • Ensure all clinical data management tasks are complete prior to database lock.
  • Produce and/or coordinate reports and listings for team reviews and DSMBs (Data Safety Monitoring Boards).
  • Ensure the project team and the sponsor is kept informed of all issues and timelines together with quality and performance achieved.
  • Identify and recommend process improvements and standards to department management and implements approved process improvements.
  • Assists in development and review of SOPs.
  • Assist with special projects as designated by management.
  • Perform other duties as assigned by management.

Experience:
  • Proven knowledge of clinical data management process and clinical database systems
  • Excellent problem-solving, analytical, and communication skills.
  • Ability to work collaboratively in a fast-paced, team-oriented environment.
  • Strong leadership and mentorship skills.
  • Ability to work independently and manage multiple projects simultaneously.
  • Strong attention to detail and quality.
  • Extensive experience within the CRO industry
  • Extensive knowledge of Clinical Data Management System(s), including Electronic Data Capture system(s)

Education/Qualifications:
  • BS/RN in Life Sciences and/or combination of education and experience
  • Minimum of 8-10 years experience in clinical data management
  • Strong oral and written communication skills
  • Effective working knowledge of Microsoft Office Suite including Word, Excel, and Project
  • Demonstrated problem solving, analytical, organization, and time management skills
  • Demonstrated flexibility and ability to work well in a team environment
  • Demonstrated ability to be compliant with GCP/regional regulatory guidelines and SOPs

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