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Remote Clinical Data Manager Jobs in Raleigh, NC

IQVIA

Clinical Research Coordinator

Raleigh, NC · Remote

$35 - $42/hr

... manage clinical, operational, and data-related responsibilities while ensuring compliance with ... This position is not eligible for visa sponsorship #LI-CES and #LI-DNP #LI-HCP #remote IQVIA is a ...

Biodata Partners, Inc.

Senior Medical Coder

Raleigh, NC · On-site +1

$16 - $21.50/hr

Manage end-to-end delivery of clinical data management coding responsibilities concurrently for single/multiple projects ensuring quality and timeliness. Provide leadership and mentorship to Medical ...

McKesson

Clinical Science Liaison

Cary, NC · Remote

$60K - $81K/yr

Remote (U.S.-based); must reside within 30 minutes of a major airport. Preference for Dallas-Fort ... Ability to interpret and communicate complex clinical data in oncology and rare disease.

McKesson Corporation

Clinical Science Liaison

Cary, NC · On-site +1

$60K - $81K/yr

Remote (U.S.-based); must reside within 30 minutes of a major airport. Preference for Dallas-Fort ... Ability to interpret and communicate complex clinical data in oncology and rare disease.

McKesson

Clinical Science Liaison

Cary, NC · Remote

$60K - $81K/yr

Remote (U.S.-based); must reside within 30 minutes of a major airport. Preference for Dallas-Fort ... Ability to interpret and communicate complex clinical data in oncology and rare disease.

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All JobsClinical Data JobsRemote Clinical Data Manager JobsRemote Clinical Data Manager Jobs in Raleigh, NC

Remote Clinical Data Manager information

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How much do remote clinical data manager jobs pay per hour?

As of Jun 15, 2026, the average hourly pay for remote clinical data manager in Raleigh, NC is $55.57, according to ZipRecruiter salary data. Most workers in this role earn between $43.94 and $66.11 per hour, depending on experience, location, and employer.

What Does a Remote Clinical Data Manager Do?

Remote clinical data managers collect, compile, and organize data from research projects and clinical trials. They perform their job duties from home or another location outside of the office with internet capability. In this career, you are responsible for recording relevant information and results from clinical trials and making sure they are logged accurately and secured correctly. You examine the research process, checking that the data meets industry regulations and requirements for clinical testing. Once the trial begins, you evaluate the data to ensure researchers collect the right information as they conduct their tests, experiments, or research. You collaborate remotely with researchers to produce reports, statistics, and charts. Remote clinical data managers work with pharmaceutical companies, healthcare providers, government agencies, and research institutions.

What is the difference between Remote Clinical Data Manager vs Remote Clinical Research Associate?

AspectRemote Clinical Data ManagerRemote Clinical Research Associate
CredentialsBachelor's in Life Sciences, Biostatistics, or related field; experience with data management systemsBachelor's in Life Sciences, Nursing, or related field; experience in monitoring and site management
Work EnvironmentData analysis, database management, and quality controlMonitoring clinical sites, ensuring protocol adherence, and site communication
Industry UsagePharmaceutical, biotech, and clinical research organizationsPharmaceutical, biotech, and contract research organizations
Search & Comparison IntentFocuses on data management roles in clinical trialsFocuses on site monitoring and trial oversight roles

The main difference is that Remote Clinical Data Managers handle data collection, validation, and database management, while Remote Clinical Research Associates focus on site monitoring and ensuring trial compliance. Both roles are essential in clinical research but serve different functions within the trial process.

What are the key skills and qualifications needed to thrive as a Remote Clinical Data Manager, and why are they important?

To thrive as a Remote Clinical Data Manager, you need expertise in clinical data management, knowledge of regulatory guidelines (such as GCP), and a degree in life sciences or a related field. Familiarity with electronic data capture (EDC) systems, clinical trial management software, and certifications like CCDM are typically required. Strong attention to detail, problem-solving abilities, and effective remote communication skills help you excel in this position. These competencies ensure accurate data collection, regulatory compliance, and efficient collaboration within dispersed clinical research teams.

How does a Remote Clinical Data Manager typically collaborate with clinical research teams and ensure data integrity across different locations?

As a Remote Clinical Data Manager, you'll frequently coordinate with cross-functional teams, including clinical research associates, biostatisticians, and project managers, using digital communication tools and project management platforms. Ensuring data integrity involves setting up secure data management systems, implementing data validation checks, and conducting regular data reviews. You'll participate in virtual meetings to discuss data queries, timelines, and protocol updates, and often provide training or support to site staff on electronic data capture (EDC) systems. Maintaining clear communication and thorough documentation is essential for successful remote collaboration and high-quality data management.

What is a Remote Clinical Data Manager?

A Remote Clinical Data Manager is a professional responsible for overseeing the collection, processing, and management of clinical trial data while working from a remote location. They ensure that the data collected during clinical studies is accurate, complete, and compliant with regulatory standards. Their key tasks include database design, data cleaning, and collaborating with clinical teams to resolve data discrepancies. Remote Clinical Data Managers often use specialized software and work closely with other research professionals to maintain data integrity and support successful clinical trial outcomes.
More about Remote Clinical Data Manager jobs
What are the most commonly searched types of Remote Clinical Data jobs in Raleigh, NC? The most popular types of Remote Clinical Data jobs in Raleigh, NC are:
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What job categories do people searching Remote Clinical Data Manager jobs in Raleigh, NC look for? The top searched job categories for Remote Clinical Data Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Remote Clinical Data Manager jobs? Cities near Raleigh, NC with the most Remote Clinical Data Manager job openings:
Remote Clinical Data Manager jobs near you
Infographic showing various Remote Clinical Data Manager job openings in Raleigh, NC as of June 2026, with employment types broken down into 90% Full Time, 5% Temporary, and 5% Contract. Highlights an 100% Remote job distribution, with an average salary of $115,582 per year, or $55.6 per hour.

Principal Clinical Data Manager

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Contractor

Posted 23 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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