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Entry Level Clinical Data Manager Jobs in Raleigh, NC

Manager, Database Management Systems Job Summary Seeking an experienced clinical data professional ... This role will serve as a subject matter expert in clinical data standards, Medidata Rave global ...

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 ... Managers and supervisors may assign other duties as needed. Required Knowledge, Skills, and ...

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 ... Managers and supervisors may assign other duties as needed. Required Knowledge, Skills, and ...

... data management plans, data transfer plans, and clinical data review activities. " Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics, and other ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

... data integrity and GCP compliance. • Provide clinical input into case report forms, data management plans, data transfer plans, and clinical data review activities. • Collaborate with data ...

Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics, and other functional groups to support effective study execution. * Prepare key reports on study ...

Collaborate with data management, safety, regulatory, clinical supplies, contracts, biostatistics, and other functional groups to support effective study execution. * Prepare key reports on study ...

... data (eg, Prism files, bioanalytical reports, clinical pathology reports, PK/TK evaluation reports) * Collaborate with cross-functional teams such as project management, safety, efficacy, biostats ...

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Entry Level Clinical Data Manager information

See Raleigh, NC salary details

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How much do entry level clinical data manager jobs pay per hour?

As of Jul 14, 2026, the average hourly pay for entry level 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 an Entry Level Clinical Data Manager do?

An Entry Level Clinical Data Manager is responsible for collecting, organizing, and ensuring the accuracy of data generated during clinical trials. They work closely with clinical research teams to input data into specialized databases, perform quality checks, and help resolve discrepancies. Their role is essential in maintaining data integrity and supporting the successful completion of medical research studies. Entry-level positions often involve learning industry regulations, data management systems, and standard operating procedures under the guidance of more experienced staff.

What Does an Entry-Level Clinical Data Manager Do?

An entry-level clinical data manager compiles and organizes information from medical research projects, such as clinical trials and pharmaceutical tests. In this role, you collect, process, and input the information from these trials into your company's database while ensuring all the data you handle are accurate and secure. The information must be stored and organized to enable the researchers and medical professionals to analyze and interpret the findings. You may also assist research teams in finding specific pieces of data and collaborate with medical groups to meet grant application deadlines or publication guidelines. Because this is an entry-level position, you may work under an experienced data manager until you can handle your responsibilities on your own.

What are some common challenges faced by entry level clinical data managers during their first year on the job?

As an entry level clinical data manager, you may encounter challenges such as learning to navigate complex clinical trial data management systems, ensuring data accuracy while meeting tight deadlines, and understanding regulatory compliance requirements. Adapting to the fast-paced environment and collaborating effectively with cross-functional teams, including clinical research associates and statisticians, can also be demanding initially. However, with mentorship and on-the-job training, these challenges become valuable learning opportunities that help build a solid foundation for a career in clinical data management.

What are the key skills and qualifications needed to thrive as an Entry Level Clinical Data Manager, and why are they important?

To thrive as an Entry Level Clinical Data Manager, you need a solid understanding of clinical research processes, data management principles, and a relevant degree such as life sciences or statistics. Familiarity with clinical data management systems (CDMS), electronic data capture (EDC) tools like Medidata Rave, and GCP certification are typically expected. Attention to detail, analytical thinking, and effective communication are essential soft skills for ensuring data quality and collaborating with study teams. These competencies are crucial for maintaining data integrity, regulatory compliance, and supporting successful clinical trials.

What is the difference between Entry Level Clinical Data Manager vs Clinical Data Coordinator?

AspectEntry Level Clinical Data ManagerClinical Data Coordinator
CredentialsBachelor's in life sciences or related field; familiarity with data management toolsBachelor's in health sciences or related field; basic data entry skills
Work EnvironmentPharmaceutical or biotech companies, CROs, clinical research settingsClinical trial sites, hospitals, research organizations
ResponsibilitiesManaging data collection, quality control, database setupData entry, data verification, supporting data queries

Entry Level Clinical Data Managers and Clinical Data Coordinators often work in clinical research environments, but the former typically handles data management systems and quality control, while the latter focuses on data entry and verification. Both roles require similar educational backgrounds, but the Clinical Data Manager position involves more technical responsibilities and oversight.

What are the most commonly searched types of Clinical Data Manager jobs in Raleigh, NC? The most popular types of Clinical Data Manager jobs in Raleigh, NC are:
What job categories do people searching Entry Level Clinical Data Manager jobs in Raleigh, NC look for? The top searched job categories for Entry Level Clinical Data Manager jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Entry Level Clinical Data Manager jobs? Cities near Raleigh, NC with the most Entry Level Clinical Data Manager job openings:
Infographic showing various Entry Level Clinical Data Manager job openings in Raleigh, NC as of July 2026, with employment types broken down into 82% Full Time, 9% Part Time, and 9% Contract. Highlights an 91% In-person, and 9% Remote job distribution, with an average salary of $115,582 per year, or $55.6 per hour.
Mgr, Database Management Systems

Mgr, Database Management Systems

IQVIA, Inc.

Durham, NC • On-site

$84K - $211K/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

56th of 210 rated it services


Job description

Manager, Database Management Systems
Job Summary
Seeking an experienced clinical data professional to lead database management and clinical data standards activities supporting global clinical trials. This role will serve as a subject matter expert in clinical data standards, Medidata Rave global library development, and SAS programming, partnering with cross-functional teams to ensure high-quality, standardized clinical data collection and reporting.
Key Responsibilities
  • Lead development and maintenance of global clinical data standards, including CDISC-compliant operational data mappings and SDTM standards.
  • Build and maintain Medidata Rave global library objects, including eCRFs, edit checks, and CRF Completion Guidelines.
  • Develop SAS programs for edit checks, data imports, listings, custom reports, and clinical data validation.
  • Create and manage clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS.
  • Support CRF design, annotated CRFs, data mapping specifications, and define.xml requirements.
  • Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CRO partners to ensure consistent standards implementation.
  • Drive process improvements, support governance committees, and provide mentorship to junior team members.
  • Ensure compliance with CDISC standards, GCP, ICH guidelines, and regulatory requirements.

Required Qualifications
  • Strong clinical domain knowledge with a solid understanding of clinical trial phases.
  • Prior work experience must be within the clinical research, pharmaceutical, biotechnology, healthcare, or CRO industry.
  • Hands-on experience programming Edit Check Listings using SAS.
  • Experience with Data Import Programming using SAS.
  • Experience utilizing SAS Output Delivery System (ODS) to generate reports in RTF, PDF, and HTML formats.
  • Experience reading raw data files, creating data structures, handling missing values, troubleshooting programming errors, and managing clinical data.
  • Experience appending and concatenating SAS datasets.
  • Proficiency developing reports using PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.
  • Strong programming experience with SAS Macros and SQL.
  • Experience creating SAS datasets from raw clinical data, including status and efficacy datasets.
  • Ability to develop project-specific macros and formats, load client data from external platforms, and prepare datasets for client delivery.
  • Experience creating clinical listings and custom reports based on business requirements.
  • Knowledge of Vendor Import Programming.
  • Strong technical expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid.
  • Ability to develop code using Base SAS programs, SAS procedures, and standardized macros.
  • Excellent written and verbal communication skills.

Preferred Qualifications
  • Experience with CDASH and ADaM standards.
  • Extensive Medidata Rave global library development experience.
  • Knowledge of MedDRA, WHODrug, annotated CRFs, and data mapping specifications.
  • Experience with Veeva, Medrio, Oracle Clinical, TrialGrid, or similar EDC systems.
  • Demonstrated ability to lead cross-functional initiatives in a global clinical development environment.

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 at https://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 $84,600.00 - $211,600.00. 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.

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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