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

IQVIA

Clinical Data Manager

Durham, NC · On-site

$68K - $171K/yr

Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data ...

IQVIA

Senior Clinical Data Coordinator

Durham, NC · On-site

$50K - $126K/yr

Job Overview The Sr. Clinical Data Coordinator performs activities pertaining to the conduct of ... Perform ongoing data review, including reconciliation of third party data streams and serious ...

Duke University

Clinical Data Manager

Durham, NC · On-site

Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may ... Review external data transfer plans, and support audits, inspections, and regulatory activities ...

Duke University

Clinical Data Manager

Durham, NC · On-site

Completion of the DOCR North Carolina state approved Clinical Research Apprenticeship program may ... Review external data transfer plans, and support audits, inspections, and regulatory activities ...

Fortrea

Senior Clinical Data Manager

Durham, NC · On-site

Regularly review client specific process to ensure they remain optimal for Sponsor and Fortrea. The Senior Clinical Data Manager will work with the leadership team to provide guidance, mentoring and ...

Spectraforce Technologies

Medical Reviewer

Raleigh, NC · On-site

Act as a central link between cross-functional review committees, integrating current medical information, clinical data, and therapeutic insights into departmental resources. * Meeting Participation:

AskBio

Manager, Data Management

Durham, NC · On-site

Utilizing and developing SAS, SQL, Power BI, Excel and other analytical tools to support clinical data review, identifying data trends and discrepancies, and monitoring study performance metrics ...

New

AskBio

Manager, Data Management

Durham, NC · On-site

Utilizing and developing SAS, SQL, Power BI, Excel and other analytical tools to support clinical data review, identifying data trends and discrepancies, and monitoring study performance metrics ...

New

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance. * Provide clinical input into case report forms, data ...

System One

Clinical Study Manager

Durham, NC · On-site

Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance. * Provide clinical input into case report forms, data ...

System One

Clinical Study Manager

Durham, NC · On-site

Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance. * Provide clinical input into case report forms, data ...

Belcan

Clinical Study Manager

Durham, NC

$56.99 - $71.32/hr

Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance. * Provide clinical input into case report forms, data ...

System One

Clinical Study Manager

Durham, NC · On-site

Review clinical data, data listings, vendor reports, monitoring trends, and other study outputs to support data integrity and GCP compliance. * Provide clinical input into case report forms, data ...

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Clinical Data Reviewer information

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How much do clinical data reviewer jobs pay per hour?

As of Aug 23, 2026, the average hourly pay for clinical data reviewer in Raleigh, NC is $25.51, according to ZipRecruiter salary data. Most workers in this role earn between $14.04 and $35.29 per hour, depending on experience, location, and employer.

What is a clinical data reviewer?

A Clinical Data Reviewer is responsible for ensuring the accuracy, consistency, and integrity of clinical trial data. They review patient data in clinical databases, identify discrepancies, and collaborate with data management and clinical teams to resolve issues. Their role is critical in ensuring that trial data meets regulatory standards and supports reliable study outcomes. Clinical Data Reviewers typically have backgrounds in life sciences, clinical research, or data management.

What are the day-to-day responsibilities of a clinical data reviewer?

As a Clinical Data Reviewer, your daily tasks often include evaluating and verifying clinical trial data for completeness, consistency, and accuracy according to study protocols and regulatory requirements. You'll collaborate closely with data managers, clinical research associates, and biostatisticians to resolve discrepancies and ensure data quality. Reviewing case report forms (CRFs), providing feedback on data queries, and documenting findings are typical activities. This role requires ongoing communication and teamwork to maintain timelines and support the integrity of the clinical trial process.

What are the key skills and qualifications needed to thrive as a clinical data reviewer?

To thrive as a Clinical Data Reviewer, you typically need a background in life sciences, experience with clinical research processes, and a keen eye for detail when reviewing clinical trial data. Familiarity with electronic data capture (EDC) systems, clinical trial management systems (CTMS), and compliance frameworks like Good Clinical Practice (GCP) or CDISC standards is highly valued. Strong analytical thinking, effective communication, and the ability to collaborate across multidisciplinary teams are standout soft skills in this role. These competencies are crucial for ensuring the accuracy, reliability, and regulatory compliance of clinical data, ultimately supporting successful research outcomes.

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

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

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

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

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

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

Clinical Data Reviewer jobs near you
Infographic showing various Clinical Data Reviewer job openings in Raleigh, NC as of August 2026, with employment types broken down into 1% As Needed, 84% Full Time, 12% Part Time, and 3% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $53,060 per year, or $25.5 per hour.

Clinical Data Manager

IQVIA

Durham, NC • On-site

$68K - $171K/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 Summary

The Clinical Data Manager performs activities pertaining to the conduct of Phase I-III clinical trials in accordance with ICH/Good Clinical Practices (GCP) and other relevant procedures and guidelines. The CDM ensures, from a data management perspective, assigned trials on time, within budget, and with highest achievable quality.

Summary of the Essential Functions of the Job

  • Responsible for communicating key clinical data management metrics (e.g., data entry status, query resolution and aging, etc.) and determining appropriate actions in conjunction with study team.
  • Responsible for the review, development and/or writing of clinical trial documents and manuals, including but not limited to Case Report Forms, Edit Checks, Data Management Plans, Clinical Data Review Plans and eCRF Completion Guidelines.
  • Participate in User Acceptance Testing (UAT), as needed.
  • Participate in Quality Control (QC), as needed.
  • Responsible for working with the assigned Clinical Database Programmer(s) to ensure the development of the Data Flow Chart(s), Data Transfer Specifications and Import Guidelines.
  • Assist with site and/or third party vendor training on CDM-related topics.
  • 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.
  • Responsible for archiving trial(s) and associated documentation upon trial(s) completion.
  • Ensure adherence to Good Clinical Practice and all applicable local and international regulations.

Minimum Requirements

  • Minimum of 5 years of data management experience is required.
  • 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.
  • 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.
  • Project management experience (within Data Management) is preferred.
  • Work history at a Clinical Research Organization (CRO) or CRO management experience in data management 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 $68,500.00 - $171,100.00. 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

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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

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