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Medidata Rave Remote Jobs in North Carolina (NOW HIRING)

Senior Programmer Analyst

Durham, NC · Remote

$80K - $95K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software ... Application Deadline:8/15/26#LI Remote Learn more about our EEO & Accommodations request here.

Senior Data Team Lead (Remote)

Charlotte, NC · Remote

$86K - $217K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

Senior Data Team Lead (Remote)

Durham, NC · Remote

$86K - $217K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

Senior Data Team Lead (Remote)

Raleigh, NC · Remote

$86K - $217K/yr

  • Medical

  • Dental

  • Vision

  • Life

  • Retirement

  • PTO

Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ... Fully remote role - company equipment provided * Competitive salary and performance-based ...

Medidata Rave Remote information

What is the difference between Medidata Rave Remote vs Clinical Data Coordinator?

AspectMedidata Rave RemoteClinical Data Coordinator
Required CredentialsExperience with Medidata Rave, clinical data management certificationsDegree in life sciences, training in data management systems
Work EnvironmentRemote, primarily computer-basedOffice or remote, depending on employer
Industry UsageUsed by clinical research organizations and pharma companiesCommonly employed in clinical trial sites and CROs

Medidata Rave Remote specialists focus on managing clinical trial data using Medidata Rave software, often working remotely. Clinical Data Coordinators handle data entry, validation, and management at trial sites or offices. While both roles involve clinical data, Medidata Rave Remote roles require specific software expertise, whereas Clinical Data Coordinators focus on data quality and compliance in clinical settings.

What are the key skills and qualifications needed to thrive as a Medidata Rave remote specialist?

To excel as a Medidata Rave Remote Specialist, you need a solid understanding of clinical data management, electronic data capture (EDC) systems, and often a background in life sciences or related fields. Familiarity with the Medidata Rave platform, GCP compliance, and certification in Medidata Rave or similar EDC systems are typically required. Strong analytical thinking, attention to detail, and effective communication skills help professionals manage clinical trial data accurately and collaborate with remote teams. These competencies ensure high-quality data integrity, regulatory compliance, and smooth clinical trial operations in a remote environment.

What are some common challenges faced by remote Medidata Rave professionals, and how can they overcome them?

Remote Medidata Rave professionals often encounter challenges such as coordinating with global clinical teams across time zones and ensuring secure, accurate data entry and management. Communication can be more complex when troubleshooting database issues or implementing protocol amendments from a distance. To overcome these hurdles, it's important to establish clear communication channels, maintain detailed documentation, and participate in regular virtual meetings with study stakeholders. Familiarity with collaborative tools and Medidata Rave's support resources can also help streamline remote workflows and resolve technical issues efficiently.

What is a Medidata Rave remote?

A Medidata Rave remote job involves working with the Medidata Rave clinical data management system from a location outside of a traditional office, typically from home or another remote setting. Professionals in these roles are responsible for building, managing, or supporting electronic data capture (EDC) systems used in clinical trials. Remote positions can include roles such as database developers, clinical data managers, or support specialists, all of whom collaborate virtually to ensure data integrity and regulatory compliance in clinical research. These jobs require strong familiarity with Medidata Rave software, attention to detail, and effective communication skills for remote teamwork.
What are popular job titles related to Medidata Rave Remote jobs in North Carolina? For Medidata Rave Remote jobs in North Carolina, the most frequently searched job titles are:
What job categories do people searching Medidata Rave Remote jobs in North Carolina look for? The top searched job categories for Medidata Rave Remote jobs in North Carolina are:
Infographic showing various Medidata Rave Remote job openings in North Carolina as of August 2026, with employment types broken down into 92% Full Time, and 8% Contract. Highlights an 100% Remote job distribution.

Senior Programmer Analyst

Fortrea

Durham, NC • Remote

$80K - $95K/yr

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 6 days ago


Fortrea rating

8.3

Company rating: 8.3 out of 10

Based on 11 frontline employees who took The Breakroom Quiz

26th of 73 rated research


Job description

Job Overview:

Lead the development and implementation of solutions to global technical services issues and concerns regarding EDC tools like Medidata RAVE or Oracle Inform or Data/Report programming or Visual Analytics tools like Spotfire or Tableau. Develop/validate Custom/Complex SAS / SDTM datasets and efficiently handle external data and reconciliations. Perform any postproduction changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, SAS Datasets etc., Conduct Peer Review/Quality control of study design for assigned projects.

    Summary of Responsibilities:

    • Lead the development and implementation of Clinical solutions to global technical services issues and concerns regarding EDC tools or SAS programming.
    • Lead the development of visual analytics dashboard using tools like Spotfire/Tableau.
    • Complete assigned work utilizing Medidata Rave or Oracle Inform or other proprietary software according to Fortrea SOPs, Work Instructions, and project specific guidelines in accordance with Good Clinical Practices.
    • Perform any post-production changes to the EDC database or enhancements to the SAS programs like SAS edit checks, listings, Protocol Deviations, etc.,
    • With assistance, meet with Data Manager on assigned projects to discuss contractual obligations and timelines.
    • Act as Subject Matter Expert (SME) and be point of contact for any technical services, issues related to EDC tools or SAS programming.
    • Serve as Lead Statistical Programmer providing programming support for development and maintenance of SDTM/Client standards datasets.
    • Develop/validate Custom/Complex SDTM domains and efficiently handle external data and data reconciliations.
    • Develop and implement SDTM automation/standardization and best programming practices across projects to enhance quality and productivity.
    • Plan, execute and oversee all programming activities on a study, including but not limited to, resource estimation, meeting timelines, maximizing quality, interaction with other departments and the client, etc.
    • Exhibit good imparting, analytical skills along with testing, troubleshooting, error fixing, and documentation skills.
    • Participate in the ongoing review of the processes used to ensure adaptation of best practices.
    • Conduct Peer Review/Quality control of study design for assigned projects.
    • Able to work independently and take initiative to accept new challenges in Clinical Programming Applications, also participate in the validation of new or updates to software.
    • Maintain awareness of new developments in EDC products which may be applied to improve the efficient use of these systems.
    • Resource forecasting and allocate activities to the team members on the project.
    • Proactively identify trends, generate reports/metrics, or demonstrate programming processes to sponsors/auditors (if required), assist with the design of ECRFs and other study documents.
    • And all other duties as needed or assigned

    Qualifications (Minimum Required):

    • University / college degree (life sciences, health sciences, information technology or related subjects preferred).
    • Experience and/or education plus relevant work experience, equating to a bachelor's degree will be accepted in lieu of a bachelor's degree.
    • Fluent in English, both written and verbal.
    • Fortrea may consider relevant and equivalent experience in lieu of educational requirements.

    Experience (Minimum Required):

    • 5 to 8 years of relevant work experience to include data management and database support or SAS Programming or Spotfire or Tableau development.
    • Good problem-solving skills and a proactive approach.
    • Good oral and written communication skills.
    • Basic knowledge of clinical trial process and data management, biometrics, and systems applications to support operations preferred.
    • Demonstrated ability to work in a team environment.
    • Demonstrated ability to work independently under supervision.
    • Proven interpersonal skills.

    Physical Demands/Work Environment:

    • Office work environment.
    Pay Range:$80,000-$95,000Benefits:All job offers will bebased on a candidate's skills and prior relevant experience, applicabledegrees/certifications,as well as internal equity and market data.Regular,full-timeor part-time employees working 20 or more hours per week are eligible for comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.Application Deadline:8/15/26#LI Remote

    Learn more about our EEO & Accommodations request here.


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