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

Fortrea

Associate Clinical Data Manager

Durham, NC · On-site

Regularly review client specific process to ensure they remain optimal for Sponsor and Fortrea ... Perform reconciliation of the clinical database against safety data, laboratory data or any other ...

New

Fortrea

Associate Clinical Data Manager

Durham, NC · On-site

Regularly review client specific process to ensure they remain optimal for Sponsor and Fortrea ... Perform reconciliation of the clinical database against safety data, laboratory data or any other ...

New

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:

Pharpoint Research

Principal Data Manager

Durham, NC · On-site

Perform the execution of Clinical Data Management functions with delegated authority. Serve as lead ... Review study-specific documentation as part of the project team to obtain understanding of study ...

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 ...

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 ...

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 ...

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 ...

TalentBurst, Inc.

Clinical Study Manager

Durham, NC

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 ...

Actalent

Clinical Trial Manager

Durham, NC

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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All JobsClinical Data Reviewer JobsClinical Data Reviewer Jobs in Raleigh, NC

Clinical Data Reviewer information

See Raleigh, NC salary details

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How much do clinical data reviewer jobs pay per hour?

As of Aug 9, 2026, the average hourly pay for clinical data reviewer in Raleigh, NC is $25.48, according to ZipRecruiter salary data. Most workers in this role earn between $13.99 and $35.24 per hour, depending on experience, location, and employer.

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 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 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, 80% Full Time, 13% Part Time, and 6% Contract. Highlights an 87% Physical, 3% Hybrid, and 10% Remote job distribution, with an average salary of $53,001 per year, or $25.5 per hour.

Principal Clinical Data Manager

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Contractor

Re-posted 18 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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