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Medidata Rave Database Programmer Jobs (NOW HIRING)

Medix™

Data Coordinator - 257098

New Haven, CT · On-site

... databases. 2. Ability to coordinate patient/study participant care from the recruitment phase ... Knowledge of Oracle software, Medidata Rave, EPIC and ONCORE. Knowledge of federal regulations for ...

CSL Plasma Inc.

Senior Programmer, EDC Systems

Waltham, MA · On-site

$143K - $169K/yr

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 ...

CYNET SYSTEMS

Clinical Data Management Analyst

Irvine, CA · On-site

$38.76 - $43.76/hr

Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

CYNET SYSTEMS

Clinical Data Management Analyst

Irvine, CA · On-site

$38 - $43/hr

Experience with EDC (Electronic Data Capture) systems required, both Classic and New Medidata RAVE ... We deliver agile, scalable talent solutions across IT, engineering, life sciences, clinical, and ...

Immunocore

$121K - $202K/yr

... by Clinical Programming and Biostatistics. Key Responsibilities: • Lead the development ... of EDC database builds (e.g., Medidata Rave, Veeva) to ensure adherence to global collection ...

Nexa Trials

Data Architect

Austin, TX · On-site

$63.25 - $81.25/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 ...

Everest Clinical Research Services Inc.

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

One year clinical database design experience, such as developing clinical databases in DFdiscover, InForm, Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience ...

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

As of Sep 13, 2026, the average hourly pay for medidata rave database programmer in the United States is $43.91, according to ZipRecruiter salary data. Most workers in this role earn between $33.65 and $44.47 per hour, depending on experience, location, and employer.

What is a Medidata Rave Database Programmer?

A Medidata Rave Database Programmer is a specialized IT professional who designs, builds, and manages clinical trial databases using the Medidata Rave platform. They are responsible for setting up electronic data capture (EDC) systems, creating case report forms (CRFs), implementing edit checks, and ensuring data quality for clinical studies. Their work is essential for pharmaceutical and biotech companies conducting clinical trials, as accurate data collection and management are crucial for regulatory compliance and successful study outcomes.

What are the key skills and qualifications needed to thrive as a Medidata Rave Database Programmer?

To thrive as a Medidata Rave Database Programmer, you need expertise in clinical data management, database design, and strong knowledge of electronic data capture (EDC) systems, especially Medidata Rave, often supported by a degree in life sciences or information technology. Proficiency with Medidata Rave tools, Rave EDC, edit checks, custom functions, and familiarity with CDISC standards and SQL are typically required, and Medidata certifications are highly valued. Attention to detail, analytical thinking, and effective communication are crucial soft skills for ensuring data quality and collaborating with clinical teams. These skills ensure the accurate setup, maintenance, and validation of clinical trial databases, which are vital for regulatory compliance and reliable study outcomes.

What are some common challenges faced by Medidata Rave Database Programmers, and how can they be addressed?

Medidata Rave Database Programmers often encounter challenges such as managing complex clinical trial protocols, ensuring data integrity, and meeting tight project timelines. Navigating frequent mid-study changes and adapting to evolving sponsor requirements can also be demanding. These challenges are best addressed by maintaining strong communication with clinical teams, staying updated on Medidata Rave's latest features, and following standardized programming practices to ensure quality and compliance. Collaborating closely with data managers and proactively identifying potential data issues can further help streamline project delivery.

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

AspectMedidata Rave Database ProgrammerClinical Data Coordinator
Primary RoleDesigns, develops, and maintains electronic data capture (EDC) systems using Medidata Rave.Manages and oversees data collection, entry, and quality in clinical trials.
Required SkillsKnowledge of Medidata Rave, database management, programming, and clinical trial processes.Data management, attention to detail, communication, and familiarity with clinical data workflows.
Work EnvironmentTypically works in clinical research organizations or pharmaceutical companies, focusing on EDC systems.Works in clinical trial sites or CROs, coordinating data collection and quality assurance.

While both roles are involved in clinical data management, the Medidata Rave Database Programmer specializes in developing and maintaining Rave databases, whereas the Clinical Data Coordinator focuses on managing and ensuring the quality of clinical data collection.

What are popular job titles related to Medidata Rave Database Programmer jobs?

For Medidata Rave Database Programmer jobs, the most frequently searched job titles are:

Infographic showing various Medidata Rave Database Programmer job openings in the United States as of August 2026, with employment types broken down into 88% Full Time, 7% Part Time, and 5% Contract. Highlights an 86% Physical, 4% Hybrid, and 10% Remote job distribution, with an average salary of $91,329 per year, or $43.9 per hour.

Data Coordinator - 257098

New Haven, CT • On-site

Medix™
501 - 1,000 employees
Learn more about Medix™external

Other

Posted 21 days ago

Job description

Public - Responsibilities


The Data Coordinator will provide office with direct

clinical and data management support related to the conduct of clinical trials and the

collection and reporting of study-related clinical data for clinical studies within the

assigned disease team or area. Using independent judgment and high-level decision-

making, this position is responsible for data entry, monitoring visits, and patient

scheduling for assigned disease team trials.


Public - Required Skills


Required Education and Experience Two years of related work experience in the

same job family and a Bachelore's degree in a related field; or an equivalent combination

of experience and education.


Required Skills and Abilities

1. Intermediate to advanced computer proficiency with Excel, Word and ability to utilize

electronic medical databases.

2. Ability to coordinate patient/study participant care from the recruitment phase through

off treatment and follow up phase. This coordination may require the scheduling and

verification of appointments.

3. Ability to independently and accurately abstract, create, and maintain a study

participant’s research record ensuring all required data is collected, source verified, and

entered into sponsor databases.

4. Impeccable interpersonal skills and the ability to work as a team as well as

independently while self-motivating. Professional appearance and manner as well as an

excellent attendance record. Experience working with study sponsor personnel a plus.

5. Proven ability to multitask, maintain confidentiality and manage a broad variety of

duties and shifting priorities in a changing environment and to be organized and

meticulous with details.


Public - Preferred Skills


Preferred Education, Experience and Skills

Experience coordinating, planning or working in a high-volume multi-task setting.

Knowledge of Oracle software, Medidata Rave, EPIC and ONCORE. Knowledge of

federal regulations for HIPAA and IRB. Experience working in a Clinical Trials setting

preferred. Oncology experience. Completion of Good Clinical Practice (GCP) training.

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