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Manager Clinical Data Management Jobs in Raleigh, NC

IQVIA

Senior Data Team Lead (Remote)

Raleigh, NC · Remote

$86K - $217K/yr

Lead data management for complex, global clinical trials from study setup to database lock. * Serve as the main client contact for all data management deliverables. * Oversee SAE, PK, and external ...

Belcan

Clinical Study Manager

Durham, NC · On-site

$56.99 - $71.32/hr

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

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 ...

Worldwide Clinical Trials

Clinical Scientist

Durham, NC · On-site +1

Collaborate with Data Management on CRF design, CRF instructions, and data quality plans. * Review data-driven sections of regulatory and clinical reporting documents (e.g., CSRs, INDs, NDAs/BLAs ...

IQVIA

Mgr, Database Management Systems

Durham, NC · On-site

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Essential Functions Clinical Data Standards & Operational Mapping * Participate in the development ...

IQVIA

Mgr, Database Management Systems

Durham, NC · On-site

Mgr, Database Management Systems Designs or modifies data models to solve complex database ... Essential Functions Clinical Data Standards & Operational Mapping * Participate in the development ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

Kimley-Horn

Data Management Analyst

Raleigh, NC · On-site

Overview Join our team as a Data Governance Analyst and assist the Data Governance Manager with development and implementation of robust data governance policies, standards, and practices across our ...

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Showing results 21-40

All JobsClinical Data Management JobsManager Clinical Data Management JobsManager Clinical Data Management Jobs in Raleigh, NC

Manager Clinical Data Management information

See Raleigh, NC salary details

$19

$55

$79

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

As of Sep 10, 2026, the average hourly pay for manager clinical data management 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 are the roles and responsibilities of a manager clinical data management?

A Manager of Clinical Data Management oversees the collection, processing, and quality assurance of clinical trial data to ensure accuracy and regulatory compliance. They lead teams of data managers, develop data management plans, and coordinate with clinical and regulatory teams to resolve data discrepancies. Their responsibilities often include implementing data standards, ensuring data integrity, and supporting audits and submissions to regulatory authorities. This role requires strong leadership skills, attention to detail, and expertise in clinical trial processes and data management systems.

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

To thrive as a Manager Clinical Data Management, you typically need a strong background in life sciences, clinical research, and data management, often supported by a relevant degree and experience in clinical trials. Expertise with clinical data management systems (such as Medidata Rave or Oracle Clinical), knowledge of CDISC standards, and certifications like CCDM are highly valued. Strong leadership, attention to detail, and effective communication are crucial soft skills for coordinating teams and ensuring data integrity. These skills are essential to ensure high-quality, compliant clinical data that supports successful regulatory submissions and advances clinical research.

What are some typical challenges faced by a manager clinical data management, and how can they be addressed?

Managers in Clinical Data Management often face challenges such as ensuring data quality across multiple clinical sites, meeting tight regulatory deadlines, and coordinating cross-functional teams including data analysts, clinical operations, and biostatisticians. To address these challenges, strong project management skills, proactive communication, and the implementation of robust data validation procedures are essential. Additionally, staying up-to-date with evolving regulatory requirements and investing in team training can help maintain data integrity and streamline workflows.

What is the difference between Manager Clinical Data Management vs Clinical Data Coordinator?

AspectManager Clinical Data ManagementClinical Data Coordinator
ResponsibilitiesOversees data management processes, manages teams, ensures data quality and complianceCollects, enters, and verifies clinical trial data, supports data cleaning
Required SkillsProject management, leadership, data management expertiseAttention to detail, data entry, basic understanding of clinical data
CertificationsCDMP, SAS, or related certifications often preferredTypically no advanced certifications required
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsSimilar settings, often working under supervision of managers

While both roles involve clinical data, the Manager Clinical Data Management leads data strategies and teams, whereas the Clinical Data Coordinator focuses on data entry and verification tasks. The manager role requires more leadership and strategic skills, while the coordinator role is more operational and detail-oriented.

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

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

What cities near Raleigh, NC are hiring for Manager Clinical Data Management jobs?

Cities near Raleigh, NC with the most Manager Clinical Data Management job openings:

Infographic showing various Manager Clinical Data Management job openings in Raleigh, NC as of September 2026, with employment types broken down into 100% Full Time. Highlights an 33% In-person, and 67% Remote job distribution, with an average salary of $115,589 per year, or $55.6 per hour.

Senior/Principal Clinical Programmer

Raleigh, NC • On-site, Remote

Biodata Partners, Inc.
See more jobs at Biodata Partners, Inc.external

Full-time

Re-posted 19 days ago

Job description

Job Title: Principal Clinical Programmer
Job Code: CDM0016
Department Name: Clinical Data Management
Reports to Title: Manager or above
Job Summary:
The Principal Clinical Programmer is a member of the Data Management team and serves as a subject matter expert for Clinical Data Programming, Reporting, Process, and technology. Accountable for the quality and delivery of the Data Management programming, reporting and visualization, standard, and exception data listings across studies. Scope of work includes oversight and expertise in the design, development, and validation of programs, standard and adhoc reports, standard and exception data listings, and visualizations to support ongoing data review activities, achieve critical study milestones, and gain data insights into our clinical studies. The position requires good understanding of programming methods and techniques, critical thinking, and complex problem-solving skills. This position will require strong collaboration in working with other members of the Biostatistics and Data Management, external CRO partners, and other stakeholders.
Responsibilities:
  • Serve as a subject matter expert and provide expertise for Database programming, Reporting, and Technology and optimize the use of J-Review, ETL, SAS tools, and others to support business needs.
  • Manage the quality of the data management clinical database programming deliverables including edit checks programming, complex reports, and listings; patient profiles, subject narratives, exception listings, dose modification reports, and other adhoc reports using JReview & SAS as part of standard data validation and reporting package for clinical studies.
  • Develop and/or provide oversight on the programming specifications for the data validation and reporting deliverables; code, test, and document deliverables conforming to programming standards, data quality and governance, and validation policies.
  • Partner with internal and external stakeholders to ensure timely delivery of data management programming, EDC database, external data, data management programming of reports and listings including the use of visualization tools.
  • Design and develop macros, applications, and other utilities to expedite JReview/SAS programming activities.
  • Develop standard programs, templates, reports, data listings, discrepancy reports, and patient profiles to facilitate in the ongoing review of clinical data during study conduct and study closeout.
  • Build, test, and scale-up programs for data validation derivation procedures, data reports, listings, and SAS on Demand relational database extracts for operational use, identification of data outliers, quality inconsistencies, and preparation for analysis.
  • Provide technical guidance and direct programming tasks for Medical Coding activities.
  • Provide Clinical Programming expertise and support for critical and time-sensitive study milestones including interim analysis, and database lock activities.
  • Perform ETL tasks, enhancements, validation, and maintenance of the programs and templates on an ongoing basis.
  • Perform QC, lead unit testing activities, develop validation scripts for user acceptance, manage and execute programs and dry runs as needed, and resolve programming issues proactively.
  • Develop and maintain mapping, and program specifications for standard reports, listings, and visualizations.
  • Maintain database programming checklists and trackers to ensure conformance of high-quality deliverables with the study data validation and reporting package.
  • Establish and implement programming standards and comply with regulatory requirements among project team members and across all studies.
  • Participate in the development of and ensure compliance to Standard Operating Procedures (SOPs), policies, and guidelines.

Experience:
  • Minimum of 5 years database programming experience and data validation programming in the device/pharmaceutical/CRO industry.
  • Expertise in Clinical Programming, methods, and techniques
  • Expertise in using standard reporting and data visualization tools including JReview, and SAS tools.
  • Knowledge of industry standard clinical technologies including CTMS, EDC (RAVE, InForm)
  • Knowledge of CDISC data standards.
  • Knowledge and understanding of relational databases.
  • Clinical Programming, Project Management, and Technical Expertise
  • Knowledge of logical data design and data mapping
  • Knowledge of reporting and data visualization tools: JReview, Spotfire, SAS suite and ETL technology
  • Experience with programming development, validation, execution, maintenance, documentation, and archival of clinical data for regulatory submission is required.
  • Proficient in industry standards, medical terminology, and clinical trial methodologies.

Education:
  • Bachelor of Science degree in Computer Science, Mathematics, or related area with relevant experience
  • Other degrees and certifications considered if commensurate with related data management experience

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