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Contract Medidata Rave Programmer Jobs (NOW HIRING)

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Strong hands-on experience with at least one major EDC platform (Medidata Rave preferred). * Solid ...

Celerion

EDC Developer / Programmer

OR · Remote

... 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 ...

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

... Medidata Rave). * Excellent understanding of data administration and management functions (collection, analysis, data review process, etc.). * Excellent hands on experience on SAS or R programming ...

Celerion

EDC Developer / Programmer

... 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 ...

Cytokinetics

Contract Clinical Systems Specialist

$75 - $86/hr

Bachelor's degree in information technology, computer science, computer engineering, statistics, or ... Experience with EDC (Medidata Rave) and/or clinical data repository (CDR) systems * Experience with ...

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Contract Medidata Rave Programmer information

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$68

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

As of Jun 20, 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.

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.

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 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
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Contract Medidata Rave Programmer jobs near you
Infographic showing various Contract Medidata Rave Programmer job openings in the United States as of June 2026, with employment types broken down into 1% Locum Tenens, 1% Internship, 3% Temporary, and 95% Contract. Highlights an 80% Physical, 2% Hybrid, and 18% Remote job distribution, with an average salary of $82,234 per year, or $39.5 per hour.

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite day 1

TestingXperts Inc. DBA Damcosoft

San Francisco, CA • On-site

$109K - $140K/yr

Contractor

Posted 5 days ago

Job description

LIMS ,Pharma Sr. Business Analyst/Product Owner(San Francisco, CA) Onsite

Pharma R&D Functional Expert

Location: San Francisco, CA – Onsite
Type: Contract

We are looking to engage an experienced Pharma R&D Functional Expert for one of our clients in San Francisco.

Role Overview:
The consultant will serve as the primary contact for the development of a data and analytics platform on Databricks, acting as the bridge between customer’s R&D stakeholders and the technical data engineering team. The key responsibility will be to define business rules/logic and provide clear documentation for implementation.

Key Requirements:

  • 8–10 years of experience in the pharmaceutical/biotech industry, specifically in R&D, clinical operations, or bioinformatics data management.
  • Strong communication skills to translate scientific/clinical requirements into technical specifications.
  • Experience with clinical data systems (Medidata RAVE or other EDC platforms).
  • Familiarity with CDISC standards (SDTM, ADaM) and LIMS.
  • Good understanding of clinical trial processes.

Nice to Have:

  • Exposure to genomics data (NGS, gnomAD, GWAS) and bioinformatics data lifecycle.
  • Knowledge of SAS and R in statistical/clinical reporting and regulatory submissions.
  • Experience with data platforms (data lakes, data mesh), cloud (Azure preferred), and Databricks/Spark.
  • Translational medicine experience.

Thanks and Regards,

Rajiv Kumar

Associate Manager

Corporate Office:  650 Wilson Lane, Suite 201, Mechanicsburg, PA 17055

Testingxperts Inc DBA Damcosoft

P: +1 631-759-8044  Ext 518

E: Rajiv.kumar@damcosoft.com  

https://www.linkedin.com/in/rajiv-kumar-38396310a/