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Work From Home Clinical Programmer Medidata Rave Jobs in Raleigh, NC

HMG Careers

Work From Home Sales Specialist

Wendell, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Carrboro, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Sims, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Knightdale, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Louisburg, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Pine Level, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Zebulon, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Lillington, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

HMG Careers

Work From Home Sales Specialist

Oxford, NC · Remote

$69K/yr

Remote, work-from-home career * Average first-year earnings of $69K through commissions and bonuses * Increased earning potential in later years through performance and renewals * Residual income ...

Apply Early

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All JobsClinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave Jobs in Raleigh, NC

Work From Home Clinical Programmer Medidata Rave information

See Raleigh, NC salary details

$24

$62

$99

How much do work from home clinical programmer medidata rave jobs pay per hour?

As of Jul 7, 2026, the average hourly pay for work from home clinical programmer medidata rave in Raleigh, NC is $62.97, according to ZipRecruiter salary data. Most workers in this role earn between $52.12 and $71.25 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Work From Home Clinical Programmer using Medidata Rave, and why are they important?

To thrive as a Work From Home Clinical Programmer specializing in Medidata Rave, you need a solid background in clinical data management, programming (such as SQL, SAS, or R), and a degree in life sciences or a related field. Familiarity with Medidata Rave EDC, CDISC standards (SDTM, CDASH), and certifications like Medidata Rave Certified Study Builder are often required. Strong attention to detail, problem-solving abilities, and effective remote communication are vital soft skills for excelling in this role. These competencies ensure accurate data capture, regulatory compliance, and seamless collaboration across globally distributed clinical research teams.

How does a work-from-home Clinical Programmer using Medidata Rave typically collaborate with study teams and resolve data management issues remotely?

As a remote Clinical Programmer specializing in Medidata Rave, you will frequently interact with data managers, clinical research associates, and biostatisticians through virtual meetings and collaboration tools. You'll be responsible for programming study databases, building and validating electronic case report forms (eCRFs), and troubleshooting data discrepancies. Effective communication and proactive problem-solving are key, as you may need to quickly address queries or implement changes based on feedback. Most organizations use platforms like Microsoft Teams, Slack, or email to facilitate real-time collaboration, ensuring that despite working remotely, you remain integrated with the wider study team.

What is a Work From Home Clinical Programmer Medidata Rave?

A Work From Home Clinical Programmer Medidata Rave is a professional who remotely designs, builds, and manages electronic data capture systems for clinical trials using Medidata Rave software. They are responsible for creating study databases, programming edit checks, and ensuring data integrity and regulatory compliance. These programmers work closely with clinical teams to support the collection, analysis, and reporting of clinical trial data, all while working from a remote location. Their expertise in Medidata Rave and clinical data management is essential for the successful execution of clinical studies.

What is the difference between Work From Home Clinical Programmer Medidata Rave vs Work From Home Clinical Data Coordinator?

AspectWork From Home Clinical Programmer Medidata RaveWork From Home Clinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Data Management, or related field; experience with Medidata RaveBachelor's in Life Sciences, Clinical Data Management; some roles may require certification
Work EnvironmentRemote, primarily using Medidata Rave for data entry and managementRemote or hybrid, managing data entry, cleaning, and query resolution
Employer & Industry UsagePharmaceuticals, CROs, biotech firms using Medidata RavePharmaceuticals, CROs, clinical research organizations

While both roles involve clinical data management, the Clinical Programmer focuses on configuring and programming data capture in Medidata Rave, whereas the Data Coordinator handles data entry, cleaning, and query resolution. Both roles are often remote and require similar educational backgrounds, but their specific responsibilities and tools differ.

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Work From Home Clinical Programmer Medidata Rave jobs near you
Infographic showing various Work From Home Clinical Programmer Medidata Rave job openings in Raleigh, NC as of July 2026, with employment types broken down into 67% Full Time, 23% Part Time, and 10% Contract. Highlights an 100% Remote job distribution, with an average salary of $130,969 per year, or $63 per hour.

Senior/Principal Clinical Programmer

Biodata Partners, Inc.

Raleigh, NC • On-site, Remote

Full-time

Posted 13 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