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Volunteer Clinical Programmer Medidata Rave Jobs

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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Volunteer Clinical Programmer Medidata Rave information

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

As of Jun 14, 2026, the average hourly pay for volunteer 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 is the difference between Volunteer Clinical Programmer Medidata Rave vs Clinical Data Coordinator?

AspectVolunteer Clinical Programmer Medidata RaveClinical Data Coordinator
CredentialsBasic programming knowledge, familiarity with Medidata RaveDegree in health sciences or related field, data management experience
Work EnvironmentClinical trial data management, using Medidata Rave softwareData collection, entry, and quality control in clinical settings
Employer & IndustryPharmaceutical companies, CROs, biotech firmsHospitals, research institutions, clinical trial sites

The Volunteer Clinical Programmer Medidata Rave primarily focuses on configuring and managing clinical trial data within the Medidata Rave platform, often on a volunteer basis. In contrast, a Clinical Data Coordinator handles broader data management tasks, including data entry, validation, and quality assurance. While both roles require knowledge of clinical data processes, the Programmer role emphasizes technical software skills, whereas the Coordinator role involves more administrative and oversight responsibilities.

What are the key skills and qualifications needed to thrive as a Volunteer Clinical Programmer Medidata Rave, and why are they important?

To thrive as a Volunteer Clinical Programmer Medidata Rave, you need a solid understanding of clinical data management, programming principles (such as SQL or SAS), and familiarity with clinical trial processes, often supported by a degree in life sciences, computer science, or a related field. Proficiency with Medidata Rave EDC systems, CRF design, and data validation tools, as well as knowledge of CDISC standards, are typically required. Attention to detail, problem-solving ability, and strong communication skills help ensure data integrity and effective collaboration with study teams. These competencies are crucial for delivering accurate, compliant clinical data that support successful clinical trial outcomes.

What is a Volunteer Clinical Programmer Medidata Rave?

A Volunteer Clinical Programmer Medidata Rave is an individual who assists with programming tasks related to clinical trials using the Medidata Rave electronic data capture (EDC) system, typically on a volunteer or unpaid basis. Their main responsibilities include designing and building electronic case report forms (eCRFs), programming edit checks, and ensuring data integrity within the Rave platform. They work closely with clinical data managers and study teams to support the accurate and efficient collection of clinical trial data. This role is ideal for those seeking to gain experience in clinical data management and clinical programming, especially with the widely used Medidata Rave system.

What are some common challenges faced by a Volunteer Clinical Programmer working with Medidata Rave, and how can they be addressed?

Volunteer Clinical Programmers using Medidata Rave often face challenges such as adapting to strict data standards, managing complex study protocols, and ensuring data quality within tight timelines. Since volunteers may have limited prior exposure to the organization's specific workflows, familiarizing yourself with Medidata Rave's interface and standard operating procedures is crucial. Collaborating closely with clinical data managers and IT teams can help resolve data discrepancies quickly and ensure compliance with regulatory requirements. Proactively seeking training resources and participating in team meetings will help you stay aligned with project goals and improve your technical proficiency.
What cities are hiring for Volunteer Clinical Programmer Medidata Rave jobs? Cities with the most Volunteer Clinical Programmer Medidata Rave job openings:
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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Volunteer Clinical Programmer Medidata Rave jobs near you
Senior Training Specialist (Remote)

Senior Training Specialist (Remote)

Medidata Solutions

New York, NY • On-site, Remote

Full-time

Medical, Dental, Life, Retirement, PTO

Posted 18 days ago

Job description

Location: This is a hybrid remote/in-office role.
Medidata follows a hybrid office policy in which employees who are hired for an in-person position are expected to work on site a certain number of days per week following Company policy.
About our Company:
Medidata is powering smarter treatments and healthier people through digital solutions to support clinical trials. Celebrating over 25 years of ground-breaking technological innovation across more than 38,000 trials and 12 million patients, Medidata offers industry-leading expertise, analytics-powered insights, and one of the largest clinical trial data sets in the industry. More than 1 million registered users across approximately 2,300 customers trust Medidata's seamless, end-to-end platform to improve patient experiences, accelerate clinical breakthroughs, and bring therapies to market faster. A Dassault Systèmes brand (Euronext Paris: FR0014003TT8, DSY.PA), Medidata is headquartered in New York City and has been recognized as a Leader by Everest Group and IDC. Discover more at www.medidata.com . Listen to our latest podcast, from Dreamers to Disruptors , and follow us at @Medidata.
About the Team:
As a member of the Medidata Global Education team, your mission is to support the successful implementations of client study protocols and related Instructor-Led Training -producing quality training materials and exceptional training experiences for clinical trial operations personas responsible for study fulfillment and associated patient interactions.
You will join a team of 6-8 Training Specialists who author and deliver this specialized training at live or virtual global Investigator Meetings and within related training contexts.
The primary responsibility of the Senior Training Specialist is to deliver advanced end-user technical training (in the format of web based and classroom style training) for the clinical research industry that adheres to company quality standards while adhering to specific client needs. These trainings will include a variety of formats such as, recordings, demos, formal documentation (manuals) and instructor led trainings.
Finally, you will serve as a strategic mentor to new members of the team and serve as a workflow Subject Matter Expert on Medidata's Patient Experience platform with an understanding of the end-to-end data ecosystems in clinical trials.
Responsibilities:
  • Training Delivery & Execution: Deliver and manage technical training, demonstrations, and "Train the Trainer" sessions across multiple formats (Instructor-Led/Classroom, Webinar, and Remote) for internal and external clients.
  • Product Mastery: Proactively maintain comprehensive subject matter expertise on Medidata products, including newly released features and Patient Experience product workflows, applying this knowledge directly to clinical research training.
  • Consultative Client Alignment: Conduct front-end needs assessments and work directly and proactively with clients, sponsors, and CROs to tailor highly customized training strategies, workflows, and templates for complex, multi-center global protocols.
  • Project & Priority Management: Manage logistical planning and project deliverables for multiple simultaneous training assignments with highly variable deadlines and conflicting stakeholder priorities.
  • Cross-Functional Collaboration: Build productive internal and external relationships, serving as a strategic "Voice of the Customer" to feed site and patient user-experience feedback back to Medidata Product and Engineering teams.
  • Change Management: Guide clinical trial sites and sponsors through the cultural and operational shifts of adopting decentralized clinical trial (DCT) technologies.
  • Team Leadership & Support: Aid in onboarding and mentoring new team members or those looking to familiarize themselves with new products and features.
  • Compliance & Problem Solving: Independently analyze and resolve complex training delivery problems, exercising independent judgment while adhering to standard Medidata guidelines and quality procedures under the guidance of leadership.
Qualifications:
  • Communication & Presentation: Excellent written and verbal communication skills, with a proven track record of creating and delivering presentations, manuals, and technical documentation.
  • AI-Assisted Content Strategy: Familiarity with AI-assisted documentation strategies and structured content modeling designed to enable automation, improve content reusability, and drive efficiency in training lifecycle management.
  • Audience Adaptability: Ability to differentiate and tailor nuanced training content to diverse audiences throughout an organization, including clinical site staff, programmers, marketing, and executive management.
  • Clinical SaaS Expertise: Solid understanding of the clinical research industry (pharma/device/biotech) and clinical research SaaS technologies, including knowledge of Medidata products beyond Rave or CTMS.
  • Audit & Compliance Readiness: Ability to maintain meticulous training logs, version-controlled training artifacts, and documentation that can withstand sponsor or regulatory audits.
  • Independent Execution: Strong ability to work independently, manage complex study delivery, and navigate fluid client expectations.
  • Technical & Administrative Proficiency: Technical proficiency with the MS Office suite and experience defining technical training environments for classroom settings and via standard virtual training platforms (e.g., Zoom, WebEx, Teams).
  • Travel Flexibility: Ability to travel up to 50%, including weekends and international travel as necessary.
  • Bachelor's degree required; or equivalent years of experience in a Life Sciences, Biomedical, or Clinical Trial Operations discipline with technical training and/or Analytics expertise
  • 3-5 years of experience in clinical/biomedical and/ or software development environment
  • Exposure to diverse clinical trial phases (Phase I-IV) and complex therapeutic areas (e.g., Oncology, Rare Disease) where Patient Experience platforms face unique deployment challenges.
Base pay is one part of the Total Rewards that Medidata provides to compensate and recognize employees for their work. Most sales positions are eligible for a commission on the terms of applicable plan documents, and many of Medidata's non-sales positions are eligible for annual bonuses. Medidata believes that benefits should connect you to the support you need when it matters most and provides benefits, including medical, dental, life and disability insurance, 401(k) matching, family leave, flexible paid time off; and 10 paid holidays per year.
#LI-TC1
#LI-Remote
Note: Please be on the lookout for job scams. Medidata recruiters will never ask applicants for monetary compensation, credit card, or banking details.
Equal Employment Opportunity:
In order to provide equal employment and advancement opportunities to all individuals, employment decisions at Medidata are based on merit, qualifications and abilities. Medidata is committed to a policy of non-discrimination and equal opportunity for all employees and qualified applicants without regard to race, color, religion, gender, sex (including pregnancy, childbirth or medical or common conditions related to pregnancy or childbirth), sexual orientation, gender identity, gender expression, marital status, familial status, national origin, ancestry, age, disability, veteran status, military service, application for military service, genetic information, receipt of free medical care, or any other characteristic protected under applicable law. Medidata will make reasonable accommodations for qualified individuals with known disabilities, in accordance with applicable law.
We will accept applications on an ongoing basis until we fill the position.

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