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Medidata Rave Developer Jobs (NOW HIRING)

... programmers, and clinical operations personnel. You will also independently perform and oversee ... Medidata Rave build certification a plus. * Working knowledge of an electronic data capture (EDC ...

Proficient experience using multiple languages/platforms for programming including Java R ... Coding, Medidata RAVE, IRT, RBM, PACE, Pinnacle 21, MS SharePoint, sFTP with vendors etc. Strong ...

Senior Data Engineer

Boston, MA · On-site +1

$115.20K - $156.40K/yr

Medidata Rave, Castor, REDCap) and data engineering tools (e.g. AWS S3, Glue, Athena; Databricks; Dagster; dbt) * Experience bridging clinical data management and research with enterprise practices ...

Senior Clinical Data Manager

Cambridge, MA · On-site

$131.80K - $178.30K/yr

Collaborate with internal and external partners, including Biostatistics, Statistical Programming ... Experience working with Oracle InForm and Medidata Rave * Experience using standardized medical ...

New

Experience with SAS/R, SQL programming, and data manipulation. * Familiarity with clinical trial ... Experience integrating Spotfire with clinical databases and EDC systems (e.g., Medidata RAVE ...

Bachelor's degree in Computer Science, Engineering, Life Sciences, or a related discipline (or ... Experience with Medidata Rave, SAS (Grid, Viya, 9.4), Spotfire, and Veeva TMF and RIM. * Experience ...

In this role you will work closely with the Biostatistics, Programming, and Clinical Operations ... Proficient in web-based Electronic Data Capture (such as Medidata Rave and other clinical data ...

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines ...

Clinical Data Associate

Redmond, WA · On-site

$75K - $95K/yr

Exposure to a Clinical EDC system (e.g., Medidata Rave, Veeva EDC) preferred. * SAS, Python, and R programming knowledge is a plus. * Familiarity with CDISC standards (CDASH, SDTM) and GCP guidelines ...

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Medidata Rave Developer information

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How much do medidata rave developer jobs pay per hour?

As of Jun 3, 2026, the average hourly pay for medidata rave developer in the United States is $52.84, according to ZipRecruiter salary data. Most workers in this role earn between $40.38 and $64.66 per hour, depending on experience, location, and employer.

What are the key skills and qualifications needed to thrive as a Medidata Rave Developer, and why are they important?

To thrive as a Medidata Rave Developer, you need a strong background in clinical data management, database programming, and familiarity with clinical trial processes, often supported by a bachelor's degree in life sciences, computer science, or a related field. Proficiency in Medidata Rave EDC, Rave Architect, and understanding of CDISC standards, along with certifications in Medidata Rave, are typically required. Attention to detail, problem-solving skills, and effective communication are essential soft skills for collaborating with clinical teams and ensuring data accuracy. These skills are crucial for building robust clinical trial databases that support regulatory compliance and reliable data collection in clinical research.

What are some common challenges faced by Medidata Rave Developers when customizing EDC studies, and how can they be addressed?

Medidata Rave Developers often encounter challenges related to balancing complex protocol requirements with system limitations, such as creating custom edit checks or integrating third-party data sources. Managing study amendments and maintaining data integrity during mid-study changes can also be demanding. These challenges can be addressed by thorough documentation, close collaboration with study teams and data managers, and leveraging Medidata community resources for best practices. Staying updated on the latest Medidata Rave releases and participating in regular training can also help developers efficiently handle evolving study needs.

What are Medidata Rave Developers?

Medidata Rave Developers are specialized professionals who design, build, and maintain electronic data capture (EDC) systems using Medidata Rave, a leading platform in clinical data management. They are responsible for creating study databases, designing electronic case report forms (eCRFs), programming edit checks, and ensuring compliance with regulatory standards. Their work enables clinical trial data to be collected, validated, and managed efficiently, supporting pharmaceutical and biotech companies in conducting successful clinical studies.

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

AspectMedidata Rave DeveloperClinical Data Coordinator
Primary RoleDesigning, developing, and maintaining electronic data capture (EDC) systems using Medidata RaveManaging and overseeing clinical trial data collection, entry, and quality control
Required SkillsMedidata Rave platform expertise, database management, scripting, and programming skillsData management, clinical trial processes, attention to detail, and communication skills
Work EnvironmentClinical research organizations, pharmaceutical companies, CROsClinical sites, research organizations, pharmaceutical companies

While both roles are involved in clinical data management, Medidata Rave Developers focus on building and maintaining the electronic data capture systems, whereas Clinical Data Coordinators handle data entry, validation, and quality assurance during trials. Both roles are essential in the clinical research process but differ in technical focus and responsibilities.

More about Medidata Rave Developer jobs
Infographic showing various Medidata Rave Developer job openings in the United States as of May 2026, with employment types broken down into 67% Full Time, and 33% Contract. Highlights an 67% In-person, and 33% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.
Clinical Data Manager

Full-time

Medical, Dental, Vision, Life, Retirement, PTO

Posted 16 days ago


Job description

Join us in redefining what it means to work for a CRO.
When you work at Rho, it's more than just a job-you become part of the Rho Factor. We're a proud bunch of science nerds who love tackling big challenges together. We're not your typical CRO, and we're not trying to be. Here, curiosity is encouraged, fresh approaches are welcome, and collaboration is at the heart of everything we do.
Whether you're a data wizard, analytical genius, project mastermind, or any other role, you'll fit right into the equation of the Rho Factor. Expect plenty of geeky jokes, eccentric personalities, spontaneous brainstorms, and a supportive community where people genuinely care about their work-and each other.
You'll have the opportunity to experience a thriving company with real stability - financial, workforce, and corporate, which has created a safe environment to innovate and develop over a long and rewarding career.
As our next Clinical Data Manager, you will have the opportunity to work closely with the multidisciplinary project team across the life cycle of the project to ensure data management is thoughtfully planned and delivered in a consistent, timely, and high quality manner. You will be a key contributor to project success through development and utilization of innovative tools to help automate manual tasks and identify data trends in a timely fashion and constant collaboration with project peers, particularly biostatisticians, statistical programmers, and clinical operations personnel. You will also independently perform and oversee completion of data management tasks to ensure clinical database design supports project outcomes; proactively clean clinical trial data and mitigate risks; effectively communicate data-related decisions to sponsors; and ensure data management activities follow all applicable standards and project specific procedures.
Our Clinical Data Managers will tell you, joining Rho has been one of their best career moves in terms of contentment, financial rewards and career growth, which is why we have such stability in the group!
What you'll be doing:
  • Study Design & Standards
    • Independently designs CRFs and standard documentation
    • Reviews protocols and identifies basic study plan issues
  • Study Build & Start-Up
    • Assists with data import setup and standard report development
    • Supports EDC design/testing, creates edit checks, and performs UAT
    • Drafts templates and guidelines with minimal supervision
  • Data Review, Cleaning & Reconciliation
    • Leads data review planning and execution
    • Manages query workflows and SAE reconciliation
    • Identifies trends and prepares review meeting materials
  • Data Acquisition & Integrations
    • Supports integration setup/testing and manages lab ranges
    • Handles standard vendor data and flags discrepancies
  • Reporting, Lock & Closeout
    • Executes lock checklist and data verification
    • Reviews PDF packages and supports TMF readiness
  • Quality, Risk & Compliance
    • Improves processes, updates documents, and supports audits
    • Applies RBQM and QbD principles
  • Project & Stakeholder Management
    • Manages tasks across multiple projects and timelines
    • Prepares reports, tracks KPIs, and coordinates cross-functional teams
    • Handles vendor interactions and supports change initiatives
  • Leadership & Growth
    • Onboards and mentors new team members
    • Provides informal leadership and peer support
  • General Expectations
    • Attends in-person meetings as required
    • Demonstrates Rho's Core Values and delivers excellent customer service
    • Communicates professionally and promptly
    • Maintains confidentiality and takes initiative
    • Performs other duties as assigned

Requirements
  • BA/BS degree along with at least 2-5 years of clinical data management experience and experience working in clinical trials databases in a commercially available EDC system (e.g. Rave, Medrio, RedCap, Veeva); Medidata Rave build certification a plus.
  • Working knowledge of an electronic data capture (EDC) system and CRF design principles
  • Demonstrated knowledge of data review and reconciliation process
  • Demonstrates effective analytical and problem-solving skills
  • Able to independently utilize available resources, including following Standard Operations Procedures (SOPs) and templates
  • Able to communicate clearly and effectively both written and verbal
  • Strong interpersonal skills and ability to work effectively and collaboratively within a team environment
  • Self-starter, able to work independently and have the ability to coordinate multiple activities simultaneously in support of various projects.
  • Demonstrates attention to detail and commitment to producing high quality work
  • Proficiency in MS Word, Excel, PowerPoint.

Benefits
A few more things to know about us:
Benefits: Rho provides a comprehensive benefits package for all benefit-eligible employees, which includes medical, vision, dental, HSA, FSA, EAP, life & disability insurance and 401(k). All employees are eligible for paid time off, holidays, parental leave and bereavement leave.
Flexibility: We encourage a work-life balance that allows employees to bring their best selves to work while being passionate about their lives outside work.
As required by pay transparency laws in some states, Rho provides the range of starting compensation (annual salary or hourly rate) it reasonably expects to pay for a given role. Actual compensation is influenced by a wide array of factors including but not limited to role responsibilities and location as well as candidate skill set and level of experience. The range of starting pay for this role is $70,000 to $110,000 per year.
EOE. Veterans/Disabled