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Clinical Programmer Medidata Rave Jobs (NOW HIRING)

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

MapLight Therapeutics is a clinical stage biotech company that focuses on drug discovery for ... Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management ...

Veristat

Senior Clinical Database Programmer The Senior Clinical Database Programmer will work under the ... Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio. 4 years' experience ...

Mercor

Biotech Specialist - AI Trainer

Houston, TX · On-site +1

$1.1K - $1.4K/wk

Build a realistic digital workspace using tools like Medidata Rave , Oracle Clinical One , Schrödinger Suite , and Benchling . Include study protocols, IND/NDA/BLA drafts, and lab notebooks.

Salma Health

Senior Clinical Research Coordinator

La Jolla, CA · On-site

$25.50 - $33.75/hr

The Senior Clinical Research Coordinator (CRC) is the site-level owner for the onboarding and ... Enter and verify data in electronic data capture (EDC) systems (e.g., REDCap, Medidata Rave) with ...

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

As of Jul 6, 2026, the average hourly pay for clinical programmer medidata rave in the United States is $64.77, according to ZipRecruiter salary data. Most workers in this role earn between $53.61 and $73.32 per hour, depending on experience, location, and employer.

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

To succeed as a Clinical Programmer Medidata Rave, you need a strong background in clinical data management, programming (such as SAS or SQL), and knowledge of clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Expertise in using Medidata Rave EDC, along with familiarity with CDISC standards and relevant certifications, is highly valued. Attention to detail, problem-solving ability, and effective communication are standout soft skills for this role. These competencies ensure accurate data capture, smooth collaboration with study teams, and the integrity of clinical trial results.

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

Clinical Programmers working with Medidata Rave often face challenges such as managing complex protocol requirements, ensuring data quality across large datasets, and adapting to evolving regulatory standards. Addressing these challenges usually involves staying current with system updates, maintaining clear documentation, and collaborating closely with data managers, biostatisticians, and clinical teams to resolve discrepancies efficiently. Effective troubleshooting skills and ongoing training on the Medidata Rave platform can also help streamline workflow. Being proactive in communicating potential issues and actively contributing to process improvements can set you apart and help ensure the success of clinical studies.

What is a Clinical Programmer Medidata Rave job?

A Clinical Programmer specializing in Medidata Rave is responsible for designing, developing, and maintaining electronic data capture (EDC) systems for clinical trials. They configure study databases, create edit checks, and ensure data integrity within the Medidata Rave platform. Additionally, they collaborate with clinical data managers and biostatisticians to streamline data collection and validation processes. Their role is crucial in optimizing clinical trial workflows and ensuring compliance with regulatory standards.

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What are the most commonly searched types of Clinical Programmer Medidata Rave jobs? The most popular types of Clinical Programmer Medidata Rave jobs are:
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Clinical Programmer Medidata Rave jobs near you
Infographic showing various Clinical Programmer Medidata Rave job openings in the United States as of June 2026, with employment types broken down into 5% Locum Tenens, 90% As Needed, and 5% Full Time. Highlights an 90% Physical, 1% Hybrid, and 9% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.
Sr Manager Standards & Systems

Sr Manager Standards & Systems

System One

Plainsboro, NJ • Remote

Contractor

Medical, Dental, Vision, Life, Retirement

Posted 19 days ago

Job description

Job Title: Sr Manager Standards & Systems Location: REMOTE Hours: 40.0

Overview

Responsibilities

  • Serve as the primary point of contact for activities related to “Rave Safety Gateway” implementation, developing, testing, and implementing complex edit checks and custom functions to support setup and integration.
  • Translate clinical and safety business requirements into efficient, structured programming logic.
  • Develop and maintain high-quality, reusable programming components to enhance the Genmab Global Library in compliance with data standards, processes, and governance.
  • Create VBA solutions for data validation and reconciliation across multiple Excel sheets to ensure accuracy, consistency, and compliance.
  • Validate Medidata Rave Safety Gateway (RSG) implementation components, ensuring alignment with specifications and data consistency.
  • Manage deliverables and coordinate with internal and external partners throughout the RSG implementation lifecycle.
  • Configure and maintain Rave Safety Gateway modules, including AE data flow and E2B format compatibility.
  • Develop and validate RSG Custom Functions (C#), and contribute to workflow definitions, troubleshooting, and system configuration.
  • Support development and updates for the Genmab Global CRF Library (GLIB), including form reuse, standard objects, and edit checks.
  • Perform cross-sheet validation, generate QC reports, and implement business rule checks in Excel VBA tools.
  • Own project deliverables, managing timelines, risks, issues, and stakeholder communications effectively.

Requirements

  • Bachelor’s degree or equivalent experience in a relevant field.
  • Experience configuring and maintaining Medidata Rave Safety Gateway modules and workflows.
  • Strong Excel VBA programming skills, with proven experience in data validation and reconciliation.
  • Deep understanding of RSG custom functions (C#) programming and deployment.
  • Experience developing and maintaining Genmab Global CRF Library assets and standards.
  • Ability to troubleshoot, monitor, and optimize RSG logic across study phases.
  • Excellent stakeholder management, communication, and documentation skills.
  • Knowledge of E2B data formats and safety data flow processes.
  • Ability to work independently, manage multiple priorities, and meet deadlines in a fast-paced environment.

System One, and its subsidiaries including Joulé and Mountain Ltd., are leaders in delivering outsourced services and workforce solutions across North America. We help clients get work done more efficiently and economically, without compromising quality. System One not only serves as a valued partner for our clients, but we offer eligible employees health and welfare benefits coverage options including medical, dental, vision, spending accounts, life insurance, voluntary plans, as well as participation in a 401(k) plan.

System One is an Equal Opportunity Employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex (including pregnancy, childbirth, or related medical conditions), sexual orientation, gender identity, age, national origin, disability, family care or medical leave status, genetic information, veteran status, marital status, or any other characteristic protected by applicable federal, state, or local law.

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Ref: #568-Clinical

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