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Freelance Clinical Programmer Medidata Rave Jobs

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 ...

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 freelance clinical programmer medidata rave jobs pay per hour?

As of Jul 24, 2026, the average hourly pay for freelance 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 as a Freelance Clinical Programmer specializing in Medidata Rave, and why are they important?

To excel as a Freelance Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, database design, and programming—often backed by a degree in life sciences, computer science, or a related field. Expertise in Medidata Rave EDC, CDISC standards (SDTM, CDASH), and relevant programming languages like SQL or SAS is typically required, along with certifications in Medidata Rave. Strong attention to detail, problem-solving abilities, and effective communication with cross-functional teams are vital soft skills. These competencies ensure efficient, compliant clinical trial data handling and facilitate seamless collaboration in a highly regulated environment.

What does a Freelance Clinical Programmer specializing in Medidata Rave do?

A Freelance Clinical Programmer with expertise in Medidata Rave is responsible for designing, programming, and maintaining electronic data capture (EDC) systems for clinical trials using the Medidata Rave platform. Their tasks include building and validating study databases, creating eCRFs (electronic Case Report Forms), programming edit checks, and ensuring data integrity and compliance with regulatory standards. As freelancers, they typically work on a contract basis for pharmaceutical companies, CROs, or research organizations, and must stay updated on both industry regulations and the latest Medidata Rave functionalities.

What are some typical challenges a Freelance Clinical Programmer faces when working with Medidata Rave, and how can they be managed?

Freelance Clinical Programmers working with Medidata Rave often encounter challenges such as understanding complex study protocols, handling tight timelines, and ensuring accurate data mapping across multiple studies. Since freelancers may not have immediate access to on-site teams, effective remote communication and documentation are crucial for resolving queries with data managers and sponsors. Staying updated with Medidata Rave's latest features and maintaining strong organizational skills can help manage these challenges efficiently and deliver high-quality results.
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Freelance Clinical Programmer Medidata Rave jobs near you
Infographic showing various Freelance Clinical Programmer Medidata Rave job openings in the United States as of July 2026, with employment types broken down into 75% Full Time, and 25% Contract. Highlights an 75% In-person, 3% Hybrid, and 22% 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 6 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