ZipRecruiter

Log In

1

Edc Programmer Jobs in Raleigh, NC (NOW HIRING)

IQVIA, Inc.

Mgr, Database Management Systems

Durham, NC · On-site

$84K - $211K/yr

Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CRO partners to ensure consistent standards implementation. * Drive process improvements, support ...

New

IQVIA

Mgr, Database Management Systems

Durham, NC

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 ...

New

IQVIA

Mgr, Database Management Systems

Durham, NC

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 ...

New

UCB

Digital Lead, Clinical Analytics

Raleigh, NC · On-site

$125K - $165K/yr

Theideal candidate will bring deepexpertisein data architecture, data engineering, and analytics platforms, combined with strong knowledge of clinical trial systems (e.g., EDC, CDB, external data)

UCB

Digital Lead, Clinical Analytics

Raleigh, NC · On-site

$125K - $165K/yr

The ideal candidate will bring deep expertise in data architecture, data engineering, and analytics platforms, combined with strong knowledge of clinical trial systems (e.g., EDC, CDB, external data)

All JobsEdc Programmer JobsEdc Programmer Jobs in Raleigh, NC

Edc Programmer information

See Raleigh, NC salary details

$10

$35

$61

How much do edc programmer jobs pay per hour?

As of Jul 13, 2026, the average hourly pay for edc programmer in Raleigh, NC is $35.24, according to ZipRecruiter salary data. Most workers in this role earn between $22.93 and $45.87 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive in the Edc Programmer position, and why are they important?

To thrive as an EDC Programmer, you need strong programming skills, particularly in database management systems and clinical data standards, often supported by a degree in computer science or a related field. Experience with electronic data capture (EDC) platforms such as Medidata Rave, REDCap, or Oracle InForm, as well as knowledge of CDISC standards, is highly valued. Attention to detail, effective communication, and problem-solving abilities are key soft skills for success in this role. These competencies are essential for ensuring accurate clinical trial data capture and smooth collaboration with study teams in regulated environments.

Which IT job is the highest paid?

In the IT field, roles such as Chief Information Officer (CIO), IT Director, and Cloud Architect tend to be among the highest paid, often earning six-figure salaries or more. Specialized roles like Data Scientist, Solutions Architect, and cybersecurity executives also command high compensation, especially with advanced skills and certifications in cloud platforms, security, or data analysis.

What tech jobs pay $400,000 a year?

For an EDC programmer or similar specialized tech roles, earning $400,000 annually typically requires extensive experience, advanced skills in embedded systems, and often leadership responsibilities. High-paying tech jobs at this level are usually found in senior engineering, executive, or consulting positions within technology companies or industries like aerospace, defense, or finance. Compensation may include base salary, bonuses, and stock options, especially in high-growth or large organizations.

What are some typical daily responsibilities of an EDC Programmer in a clinical trials environment?

As an EDC Programmer, your daily responsibilities often include designing and configuring electronic case report forms (eCRFs), managing database setup, performing system validations, and troubleshooting data discrepancies. You’ll collaborate closely with clinical data managers, biostatisticians, and study coordinators to ensure the system effectively supports trial protocols and regulatory requirements. Additionally, you may be responsible for providing user support and training, handling database updates, and participating in ongoing process improvements. This role is central to maintaining high data quality and supporting the operational success of clinical trials.

What is an EDC programmer?

An EDC programmer is a professional who develops and maintains electronic data capture (EDC) systems used in clinical trials and research to collect, manage, and analyze data. They typically have skills in programming languages such as SQL, SAS, or R, and work closely with data managers and clinical teams to ensure data accuracy and compliance. EDC programmers often require knowledge of regulatory standards like GCP and may hold certifications in clinical data management.

What jobs in the US pay $300,000 a year?

For an EDC programmer or similar specialized roles, annual salaries of $300,000 or more are typically found in senior or executive positions such as software engineering managers, cybersecurity directors, or senior developers with extensive experience and advanced skills. High-paying roles often require advanced certifications, leadership responsibilities, or working in high-demand industries like finance, technology, or defense. Compensation varies based on location, company size, and individual expertise.

What is an EDC Programmer job?

An EDC (Electronic Data Capture) Programmer is responsible for designing, developing, and maintaining clinical trial databases used to collect and manage study data. They work with electronic data capture systems, ensuring that case report forms (CRFs) are correctly configured and meet study requirements. EDC Programmers collaborate with clinical data managers, biostatisticians, and regulatory teams to ensure compliance with industry standards and protocols. Their role is crucial in improving data accuracy, integrity, and efficiency in clinical research.

What are popular job titles related to Edc Programmer jobs in Raleigh, NC? For Edc Programmer jobs in Raleigh, NC, the most frequently searched job titles are:
What job categories do people searching Edc Programmer jobs in Raleigh, NC look for? The top searched job categories for Edc Programmer jobs in Raleigh, NC are:
What cities near Raleigh, NC are hiring for Edc Programmer jobs? Cities near Raleigh, NC with the most Edc Programmer job openings:
Edc Programmer jobs near you

Senior/Principal Clinical Programmer

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

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

Apply