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Entry Level Clinical Data Manager Jobs in Raleigh, NC

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

TalentBurst, Inc.

Clinical Study Manager

Durham, NC

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

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

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

System One

Clinical Study Manager

Durham, NC · On-site

... 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 ...

Actalent

Clinical Trial Manager- Hybrid

Raleigh, NC · Hybrid

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

Actalent

Clinical Trial Manager- Hybrid

Durham, NC · Hybrid

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

MMS

Nonclinical Writer

Raleigh, NC · On-site

... 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

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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.

More about Entry Level Clinical Data Manager jobs
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:
Entry Level Clinical Data Manager jobs near you
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

Full-time

Posted 7 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

Mgr, Database Management Systems
Designs or modifies data models to solve complex database requirements considering business and application needs. Organizes metadata for use by teams.
Essential Functions
Clinical Data Standards & Operational Mapping
  • Participate in the development and maintenance of global clinical data standards, including operational (eCRF and non-eCRF (e.g., lab, Imaging, or ECG)) data mappings.
  • To develop operational mappings, utilize Clinical Data Interchange Standards Consortium (CDISC) Study Data Tabulation Model (SDTM), controlled terminology, and other applicable industry standards.
  • SME on operational data standards utilizing SDTM standards and CDISC controlled terminology in developing operational data standards.
  • Contributing to developing and applying smart systems and optimal approaches to support data collection.
  • Independently identify and propose process improvements while maintaining a strategic focus. Share new industry standards and best practices with project and study teams and departments as required.
  • Participate and/or lead in developing Global Clinical Data Standards and other cross-functional SOPs, Working Procedures, Guidance documents, and job aids.
  • Participate and/or lead in identifying, reviewing, evaluating, and implementing new data standards-related technologies.

Global Library Management
  • Managing work assignments to ensure timely delivery of global library objects.
  • Identify and resolve issues that may negatively impact the delivery of global library objects and escalate to leadership as needed.
  • Medidata Rave global library standard objects (e.g., eCRF forms, edit checks).
  • Build, maintain, and document the Medidata Rave global library standard objects (e.g., eCRF forms, edit checks) to facilitate the creation of study-level databases.
  • Work with Data Managers and EDC Programmers to implement new or modified global library objects (e.g., ensure DM and EDCP clearly understand global library objects).
  • Build and maintain CRF Completion Guidelines for all standard forms.

Standards Governance & Committee Support
  • Support and participate in the Standards Core Committee (SCC).
  • Partner with functional area stewards.
  • Organize standards topics to be reviewed and ensure decisions are made on time.
  • Document meeting minutes and other discussions.
  • Provide input and information to facilitate critical discussions and decisions regarding standards use and implementation.
  • Support preparation of materials for the Standards Governance Committee (SGC) and address all comments received until all objects in scope get approved.

Process Compliance & Documentation
  • Follow procedural documents and participate in reviewing and updating documents to ensure they reflect industry standards and are easily followed.
  • Communicate and reinforce content and interpretation of Kite data standards to project and study teams to ensure consistency in understanding and implementing standards across a project.

Study & Project Team Support
  • Participate in relevant study and project team meetings as standards SME and provide input for standards components, such as CRF design, CRF Completion Guidelines, programmed edit checks, Data transfer specifications, mapping specifications, and annotated CRF.
  • Liaising with and reviewing work delivered by external partners (e.g., Function Service Providers, CROs, technology providers, etc.).

Stakeholder Engagement & Leadership
  • Developing strong and productive working relationships with key stakeholders throughout CDMs, Clinical Ops, and Kite with the ability to think strategically across a broad portfolio and effectively express their views to senior management.
  • Participate and/or lead in strategic initiatives, special projects, and working groups contributing to business decisions and process changes.
  • Develop training materials and provide training on CDSM and GLIB-developed processes.
  • Provide mentoring, coaching, and escalation support to more junior personnel or contract staff, as required.
  • Representing the Company in interactions with key external partners as part of any committee or industry group.

Qualifications
Required Experience
  • Medidata RAVE experience REQUIRED
  • Medidata RAVE Custom Functions experience REQUIRED
  • C# programming experience REQUIRED
  • Standards Governance experience (CDISC) REQUIRED

Candidates whose resumes do not clearly demonstrate Medidata RAVE, Custom Functions, C#, and Standards Governance experience will not be progressed for review. These are mandatory requirements for consideration.
Minimum Qualifications
  • Meditdata MS/MA in life sciences or related discipline and 4+ years of experience in Clinical Data Standards OR
  • BS/BA in life science or related discipline and 6+ years of experience in Clinical Data Standards OR
  • High School degree and 10+ years of experience in Clinical Data Standards.

Preferred Qualifications
  • MS/MA in life sciences or related discipline and 4+ years of experience in Clinical Data Standards OR
  • At least 6 years of relevant industry experience with clinical trials and a successful track record of leading through influence, working across complex, global organizational matrices.
  • Experience in Industry Standards (e.g., CDISC) in either the collection (CDASH), tabulation (SDTM), or analysis (ADaM) models.
  • At least 8 years of clinical database developer experience in Rave with expertise in global library development and development of standard data collection objects.
  • Strong understanding of the drug development process with proven expertise in clinical trial execution and global library development/clinical database development in a global arena.
  • Strong knowledge of industry-leading EDC tools (e.g., Medidata Rave, Veeva, Medrio, Oracle, TrialGrid, etc.) and well-versed in industry trends and emerging technologies supporting data collection.
  • Understanding database and dictionary structures (e.g., MedDRA, WHODrug).
  • Experience interpreting Health Authority regulations and GCP/ICH guidelines with a strong compliance background.
  • Strong working knowledge of the overall pharmaceutical development process.
  • Strong working knowledge of SDTM and creating data mapping specifications and annotated CRFs. Knowledge of requirements of define.xml.
  • Experience in CRF design, query resolution, and general data validation.
  • Technical expertise, technical writing ability, and proficiency in Systems Development LifeCycle (SDLC) principles.
  • Excellent verbal and written communication skills, high ability to communicate standards-related issues, options, and their impact to project teams and within the department.
  • Diverse and sufficient technical expertise to be a credible interface to all global development and business partners (medical, development, commercial, regulatory & quality, etc.).
  • Influential leadership and communication capabilities with a proven ability to engage, manage, develop and inspire a geographically diverse team.

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.

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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