1

Contract Medidata Rave Programmer Jobs (NOW HIRING)

Data Architect

Austin, TX · On-site

$100 - $130/hr

... Medidata Rave, Veeva, Oracle Clinical One, and custom sponsor environments. Your work directly ... Partner with integration engineers on API contracts, event schemas, and error-handling patterns for ...

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 ...

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 ...

... Programmer . You will be responsible for administration of EDC Database including evaluation ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Clinical Research Coordinator

Tupelo, MS · On-site

$23 - $30.75/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

... Programmer . You will be responsible for administration of EDC Database including evaluation ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Clinical Research Coordinator

Southaven, MS · On-site

$22.25 - $29.50/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

... Programmer . You will be responsible for administration of EDC Database including evaluation ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Clinical Research Coordinator

Meridian, MS · On-site

$23.75 - $31.75/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Clinical Research Coordinator

Madison, MS · On-site

$19.75 - $26.25/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Clinical Research Coordinator

Pearl, MS · On-site

$21 - $27.75/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Clinical Research Coordinator

Mccomb, MS · On-site

$21 - $27.75/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

Clinical Research Coordinator

Biloxi, MS · On-site

$21.50 - $28.75/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Clinical Research Coordinator

Gulfport, MS · On-site

$24.25 - $32/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Clinical Research Coordinator

Jackson, MS · On-site

$21.25 - $28/hr

Length of contract: 4 months * Type of contract: C2C * Salary rate: 40-50 USD per hour Key Tasks ... Experience with Medidata Rave * Ability and willingness to travel on-site to support study ...

New

Showing results 21-40

Contract Medidata Rave Programmer information

See salary details

$12

$39

$68

How much do contract medidata rave programmer jobs pay per hour?

As of Aug 22, 2026, the average hourly pay for contract medidata rave programmer in the United States is $39.54, according to ZipRecruiter salary data. Most workers in this role earn between $25.72 and $51.44 per hour, depending on experience, location, and employer.

What is a Contract Medidata Rave Programmer?

A Contract Medidata Rave Programmer is an information technology specialist hired on a temporary or project basis to design, configure, and maintain clinical trial databases using Medidata Rave, a leading electronic data capture (EDC) system in the pharmaceutical and biotechnology industries. Their responsibilities typically include creating electronic Case Report Forms (eCRFs), managing edit checks, programming custom data exports, and supporting data validation activities. These programmers collaborate closely with data managers, clinical teams, and statisticians to ensure that clinical data is accurately captured and compliant with regulatory standards.

How does a Contract Medidata Rave Programmer typically collaborate with clinical data management and biostatistics teams during a study?

As a Contract Medidata Rave Programmer, you will regularly interface with clinical data managers and biostatisticians to ensure that electronic data capture (EDC) systems meet protocol specifications and study requirements. You’ll participate in requirements gathering, review case report forms (CRFs), and address data validation needs, often through meetings and collaborative platforms. Effective communication and responsiveness are crucial, as you may need to troubleshoot issues, implement mid-study changes, or clarify data logic to support study timelines. This collaborative environment helps ensure high-quality data collection and smooth study execution.

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

To thrive as a Contract Medidata Rave Programmer, you need expertise in clinical data management, EDC systems, and programming languages such as SQL or SAS, typically backed by a degree in life sciences or computer science. Proficiency with Medidata Rave, eCRF design, and understanding of CDISC standards are essential, along with relevant certifications like Medidata Rave Certified Professional. Attention to detail, analytical thinking, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills and qualifications are vital for building reliable clinical databases and supporting accurate data capture in regulated clinical trials.

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

AspectContract Medidata Rave ProgrammerClinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Research, or related field; experience with Medidata RaveBachelor's in Nursing, Life Sciences, or related; familiarity with clinical data management
Work EnvironmentContract-based, primarily remote or on-site at clinical trial sites or CROsTypically on-site at clinical research sites or hospitals, coordinating data collection
Employer & Industry UsagePharmaceutical companies, CROs, clinical research organizationsHospitals, research institutions, pharmaceutical companies

The Contract Medidata Rave Programmer focuses on configuring and maintaining electronic data capture systems using Medidata Rave, while the Clinical Data Coordinator manages data collection and quality at clinical sites. Both roles require knowledge of clinical data processes but differ in technical versus operational focus.

More about Contract Medidata Rave Programmer jobs

What cities are hiring for Contract Medidata Rave Programmer jobs?

Cities with the most Contract Medidata Rave Programmer job openings:

What are the most commonly searched types of Medidata Rave Programmer jobs?

The most popular types of Medidata Rave Programmer jobs are:

What states have the most Contract Medidata Rave Programmer jobs?

States with the most job openings for Contract Medidata Rave Programmer jobs include:

What job categories do people searching Contract Medidata Rave Programmer jobs look for?

The top searched job categories for Contract Medidata Rave Programmer jobs are:

Infographic showing various Contract Medidata Rave Programmer job openings in the United States as of August 2026, with employment types broken down into 81% Full Time, and 19% Contract. Highlights an 69% In-person, and 31% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

Data Architect

Nexa Trials

Austin, TX • On-site

$100 - $130/hr

Other

Posted 16 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

#J-18808-Ljbffr