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Contract Medidata Rave Programmer Jobs in Carteret, NJ

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 ...

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 ...

MediData

Senior Applications Engineer

Woodbridge, NJ · On-site

$114.75 - $153/hr

Medidata follows a hybrid office policy in which employees who are hired for an in-person position ... Strong presentation and communication skills, including development of service contracts * Basic ...

Medidata Solutions

Senior Applications Engineer

Iselin, NJ · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... Strong presentation and communication skills, including development of service contracts Your ...

Synectics Inc

Systems Designer / Analyst

Somerville, NJ

$50.34 - $62.93/hr

Experience with technical study build in Medidata RAVE is required. * Veeva EDC technical study ... ing, finance, healthcare, and professional services recruitment, offering both contract and ...

New

Actalent

Sr. Clinical Research Coordinator

Bronx, NY · Hybrid

$35 - $42/hr

Knowledge of EDC systems such as Medidata Rave, REDCap, or similar platforms Why Join Us ... About Actalent Actalent is a global leader in engineering and sciences services and talent ...

3ds

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 ...

3ds

TA Coordinator (contract)

New York, NY · On-site

Medidata follows a hybrid office policy in which employees who are hired for an in-person position ... Your operational efficiency directly accelerates our ability to hire the engineers, data scientists ...

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All JobsContract Medidata Rave Programmer JobsContract Medidata Rave Programmer Jobs in Carteret, NJ

Contract Medidata Rave Programmer information

See Carteret, NJ salary details

$12

$40

$69

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

As of Aug 21, 2026, the average hourly pay for contract medidata rave programmer in Carteret, NJ is $40.11, according to ZipRecruiter salary data. Most workers in this role earn between $26.11 and $52.21 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.

What job categories do people searching Contract Medidata Rave Programmer jobs in Carteret, NJ look for?

The top searched job categories for Contract Medidata Rave Programmer jobs in Carteret, NJ are:

Contract Medidata Rave Programmer jobs near you

Clinical Development Engineer (Medidata Rave / Technical Support)

Group Nine LLC

Passaic, NJ • On-site

Other

Re-posted 16 days ago

Job description

Clinical Development Engineer (Medidata Rave / Technical Support)

We are seeking a Clinical Development Support Engineer with deep technical expertise in Medidata Rave and related clinical data systems. The role involves supporting critical applications across the Clinical Development lifecycle, managing integrations, automations, and troubleshooting technical issues across application, database, and interface layers. The ideal candidate will possess a mix of domain knowledge in Life Sciences and strong technical capabilities in SQL, Python, API integrations, and modern DevOps/automation tools.

Key Responsibilities
  • Provide technical and functional support for Medidata Rave, including database-level analysis, configuration, user management, and issue resolution.
  • Conduct advanced troubleshooting and root cause analysis for incidents, service requests, and integrations across the Clinical Development ecosystem.
  • Manage support operations and ticket workflows using ServiceNow, ensuring adherence to SLAs and documentation best practices.
  • Develop, optimize, and maintain SQL scripts and stored procedures in Microsoft SQL Server for reporting, validation, and data migration.
  • Create and maintain Python scripts for automation, RPA support, and ad-hoc data processing.
  • Work with RESTful APIs for integration, authentication, and data exchange between systems.
  • Support Java-based authentication utilities (JAR files) and assist in integration troubleshooting.
  • Design dashboards and reports using Tableau to support operational and analytical reporting.
  • Perform data analysis and transformation using SAS for clinical and operational datasets.
  • Utilize Git and Bitbucket for version control and code collaboration.
  • Use Atlassian tools (Jira, Confluence, Bitbucket) for task management, documentation, and collaboration across teams.
  • Manage cron-based automation schedules using VisualCron and perform basic MS-DOS command line operations for log reviews and file management.
  • Participate in validation, change management, and release activities ensuring compliance with GxP and 21 CFR Part 11.
  • Document configurations, workflows, troubleshooting steps, and reusable scripts in Confluence or standard knowledge repositories.
Nice to Have
  • SQL (Advanced–Expert): Complex query writing, joins, and performance optimization.
  • Microsoft SQL Server (Intermediate): Stored procedures and database management.
  • Python (Intermediate): Automation scripting, RPA, and data manipulation.
  • Java (Basic): Working knowledge of authentication modules and JAR handling.
  • REST API (Intermediate): Integration, data exchange, and debugging experience.
  • Tableau (Intermediate): Dashboard and visualization development.
  • SAS (Intermediate): Statistical or operational data analysis and reporting.
  • Git (Intermediate): Branching, merging, and code version management.
  • Atlassian Suite (Intermediate): Jira (task tracking), Confluence (documentation), Bitbucket (source control).
  • VisualCron (Basic): Job scheduling, monitoring, and automation setup.
  • MS-DOS Command Line (Basic): File navigation, scripting, and log handling.
  • Experience with ServiceNow or equivalent ITSM/ticketing system.
Required Skills & Qualifications
  • Bachelor's degree in Computer Science, Life Sciences, Bioinformatics, or related discipline.
  • 4–8 years of experience in Clinical Development or Clinical Data Systems support.
  • Strong hands-on experience with Medidata Rave (front-end and back-end).
  • Excellent troubleshooting and root cause analysis skills across application and data layers.
  • Strong communication, documentation, and cross-functional collaboration skills.
Preferred Qualifications
  • Prior experience in pharmaceutical R&D or clinical data management environments.
  • Familiarity with GxP, 21 CFR Part 11, and other regulatory frameworks.
  • Exposure to cloud platforms and integration monitoring tools.
  • Experience with data visualization and automation initiatives supporting clinical operations.

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