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Medidata Rave Developer Jobs (NOW HIRING)

Nexa Trials

Data Architect

Austin, TX · On-site

$100 - $130/hr

Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle ... Collaboration with engineering teams in Lahore and QC operations in Dubai * Conference and ...

CSL Plasma Inc.

Senior Programmer, EDC Systems

Waltham, MA · On-site

$143 - $169/hr

The Senior Programmer for Data Validation supports cross-functional teams such as Statistics, Data ... Familiarity with EDC systems (e.g., Medidata Rave, Veeva Vault) and understanding of eCRF design ...

MediData

Senior Data Scientist

Manhattan, NY · On-site

$114.75 - $153/hr

About the Team Medidata AI organization is building innovative AI products based on the largest ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

Immunocore

$122 - $203/hr

... by Clinical Programming and Biostatistics. Key Responsibilities: • Lead the development ... Medidata Rave, Veeva) to ensure adherence to global collection standards. • Lead standards kick ...

Medidata Solutions

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

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Medidata Rave Developer information

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How much do medidata rave developer jobs pay per hour?

As of Sep 7, 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 is a Medidata Rave developer?

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 are the key skills and qualifications needed to thrive as a Medidata Rave developer?

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 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.

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Medidata Rave Developer jobs near you
Infographic showing various Medidata Rave Developer job openings in the United States as of August 2026, with employment types broken down into 85% Full Time, 3% Part Time, and 12% Contract. Highlights an 80% Physical, 5% Hybrid, and 15% Remote job distribution, with an average salary of $109,905 per year, or $52.8 per hour.

Data Architect

Nexa Trials

Austin, TX • On-site

$100 - $130/hr

Other

Re-posted 2 days ago

Job description

Own the clinical data layer that connects NexaSource capture, Nexa Bus integrations, and sponsor EDC systems — translating protocols and CRFs into durable, standards-aligned schemas that scale across studies.

United States Austin, TX

About the role

Nexa Trials is seeking an experienced Data Architect to design and govern the clinical data models that power our platform and services. You will sit at the intersection of eSource, EDC, and sponsor reporting — defining how data captured in NexaSource™ maps through Nexa Bus™ into Medidata Rave, Veeva, Oracle Clinical One, and custom sponsor environments.

Your work directly reduces duplicate entry, query volume, and study startup friction. You will partner with clinical operations, QC analysts, integration engineers, and AI/automation teams in Lahore to ensure every mapping decision is traceable, GCP-aligned, and maintainable across protocol amendments and multi-site rollouts.

This role is based in Austin, Texas — Nexa Trials headquarters — with flexibility for hybrid or remote work within US time zones. You will report to the Head of Data & Integrations and contribute to our standards roadmap across CDISC, OMOP, and FHIR.

Responsibilities
  • Design end-to-end data models for eSource forms, visit schedules, and Nexa Bus transfer pipelines from protocol and CRF specifications
  • Author and maintain EDC/eSource field mappings, transformation rules, and validation logic for sponsor and CRO study builds
  • Define canonical data structures that support NexaSource capture, NexaScheduler visit events, and downstream analytics
  • Apply CDISC standards (SDTM, ADaM concepts, Define-XML awareness) and evaluate OMOP/FHIR applicability for interoperability initiatives
  • Partner with integration engineers on API contracts, event schemas, and error-handling patterns for live study transfers
  • Review QC findings and query trends to identify systemic mapping gaps and recommend architectural improvements
  • Document data lineage, mapping decisions, and amendment impact assessments for audit-ready sponsor deliverables
  • Contribute to reusable mapping libraries, study templates, and governance processes that accelerate study startup
  • Mentor junior data analysts and collaborate with Clinical AI engineers on structured outputs for LLM-assisted mapping tools
Requirements
  • 5+ years of experience in clinical data architecture, EDC build, or clinical data management on Phase I–IV trials
  • Deep working knowledge of CDISC standards and practical experience translating CRFs into structured clinical datasets
  • Hands‑on experience with EDC/eSource mapping — field‑level transformations, edit checks, and cross‑form dependencies
  • Proficiency with at least two major EDC platforms (e.g., Medidata Rave, Veeva Vault CDMS, Oracle Clinical One, REDCap)
  • Strong SQL skills and familiarity with data integration patterns (REST APIs, flat‑file exchange, ETL pipelines)
  • Ability to read protocols and SAPs and translate clinical intent into implementable data specifications
  • Excellent documentation habits — mapping specs, data dictionaries, and change logs that satisfy sponsor audit expectations
  • Eligible to work in the United States
Nice to have
  • Experience with OMOP CDM, FHIR resources, or real‑world data interoperability projects
  • Exposure to NexaSource, custom eSource platforms, or site‑centric capture workflows
  • Knowledge of ICH E6(R2) GCP requirements for data integrity and ALCOA+ principles
  • Python or similar scripting for mapping validation, diff analysis, or automated spec generation
  • Prior work with CROs, mid‑size sponsors, or multi‑site network rollouts
  • Familiarity with AI‑assisted mapping or clinical NLP for document extraction
What we offer

Join a clinical technology company where data architecture decisions ship to production on live studies — not sit in enterprise backlog limbo. You will shape the foundation that Nexa Bus, NexaSource, and our QC operations depend on.

  • Competitive salary, equity consideration, and comprehensive US health benefits
  • Hybrid or remote flexibility anchored to our Austin headquarters
  • Direct influence on product data models and integration strategy
  • Collaboration with engineering teams in Lahore and QC operations in Dubai
  • Conference and certification support for CDISC, FHIR, and clinical data management credentials
  • Clear path to lead architect or Head of Data & Integrations as the portfolio grows
Location

Austin, Texas, United States Region: North America Country: United States City: Austin, TX Hybrid / remote within US time zones — periodic presence at Austin HQ

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