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Medidata Rave Programmer Jobs (NOW HIRING)

Syneoshealth

Sr. Clinical Programmer

Los Angeles, CA · On-site

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Syneoshealth

OR · On-site

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Syneoshealth

Sr. Clinical Programmer

Concord, NC · On-site

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

Syneoshealth

Sr. Clinical Programmer

New York, NY · On-site

Sr. Clinical Programmer Syneos Health is a leading fully-integrated life sciences services ... Utilizes primary development tools including Medidata, Rave, Oracle OC/RDC, Oracle Inform, and/or ...

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 ...

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 ...

Frontier Science

SDTM Specialist

Buffalo, NY · On-site

The SDTM (Study Data Tabulation Model) Specialist is part of the ACTG and IMPAACT Medidata Rave ... Work directly with the statistician and programmer who is responsible for the ADaM datasets Reports ...

Prometrika LLC

Senior Clinical Data Manager

Cambridge, MA · On-site

$144K - $167K/yr

Work with DB programmers to design (e)CRFs and edit checks in EDC system for complex studies * Lead ... Expertise with EDC systems, such as Medidata Rave, InForm, Medrio * Excellent organizational and ...

3ds

Senior Training Specialist (Remote)

New York, NY · On-site +1

... Medidata Product and Engineering teams. * Change Management: Guide clinical trial sites and ... products beyond Rave or CTMS. * Audit & Compliance Readiness: Ability to maintain meticulous ...

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How much do medidata rave programmer jobs pay per hour?

As of Jul 8, 2026, the average hourly pay for 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 are some typical daily tasks for a Medidata Rave Programmer?

As a Medidata Rave Programmer, your daily tasks often involve designing and programming electronic case report forms (eCRFs), managing edit checks, and customizing the study database in the Medidata Rave platform. You'll collaborate closely with clinical data managers, biostatisticians, and other stakeholders to ensure accurate data capture and compliance with study protocols. Routine responsibilities may also include troubleshooting technical issues, validating builds, and supporting user testing. This role offers a balance of independent programming work and teamwork, providing opportunities to contribute directly to successful clinical trials.

What are the key skills and qualifications needed to thrive in the Medidata Rave Programmer position, and why are they important?

To thrive as a Medidata Rave Programmer, you need strong programming skills, experience in electronic data capture (EDC) for clinical trials, and a background in life sciences or a related field. Expertise with Medidata Rave software, familiarity with Rave Architect, and knowledge of relevant clinical data standards or CDISC certification are highly valuable. Attention to detail, effective communication, and problem-solving abilities help you excel in both independent and collaborative environments. These skills and qualities ensure accurate database builds, smooth study execution, and successful teamwork within clinical research settings.

What is a Medidata Rave Programmer job?

A Medidata Rave Programmer is responsible for designing, developing, and managing electronic data capture (EDC) systems using Medidata Rave, a widely used clinical trial software. They create study databases, build edit checks, program custom functions, and ensure data integrity for clinical trials. Their role is essential in streamlining data collection, validation, and reporting for regulatory compliance and efficient trial management.

More about Medidata Rave Programmer jobs
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 Medidata Rave Programmer jobs? States with the most job openings for Medidata Rave Programmer jobs include:
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Medidata Rave Programmer jobs near you
Infographic showing various Medidata Rave Programmer job openings in the United States as of July 2026, with employment types broken down into 1% Internship, 33% Full Time, 54% Part Time, 1% Contract, and 11% Nights. Highlights an 81% Physical, 2% Hybrid, and 17% 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

Re-posted 22 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/