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Volunteer Clinical Programmer Medidata Rave Jobs

CYNET SYSTEMS

Clinical Data Manager

Sunnyvale, CA · On-site

$70 - $75/hr

Clinical data review and listing experience (Preferably Medrio, Medidata Rave). * Excellent ... Excellent hands on experience on SAS or R programming language for data review listings/tracker.

Mercor

Drug Discovery Specialist - AI Trainer

San Jose, CA · On-site +1

$1K - $1K/wk

Represent platforms like Medidata Rave , Oracle Clinical One , Schrödinger Suite , and Benchling . * Design multi-step tasks grounded in your real workflows. Require navigating multiple apps, files ...

New

Cape Fox SS

Research Database Developer

Cincinnati, OH · Remote

$90K - $120K/yr

... within clinical research settings. The ideal candidate will possess proficiency in programming ... platforms like REDCap, Medidata Rave, Microsoft Access, and SQL-based systems. A thorough ...

Immunome, Inc.

Senior EDC Programmer

Bothell, WA · On-site

$115K - $150K/yr

Position Overview The Senior EDC (Electronic Data Capture) Programmer (Sr. EDCP) is responsible for ... Medidata Rave preferred). * Solid understanding of clinical trial processes and data flow.

Vor Bio

Senior Data Manager

Boston, MA · On-site

... programming. Suggest design for standard and non-standard data collection, identify any gaps in ... clinical data management systems and/or EDC products e.g. Medidata Rave. Must have Medidata RAVE ...

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All JobsVolunteer Clinical Programmer Medidata Rave Jobs

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 15, 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.
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Volunteer Clinical Programmer Medidata Rave jobs near you
Associate Director, Clinical Data Programmer

Associate Director, Clinical Data Programmer

Amylyx Pharmaceuticals

Cambridge, MA • Remote

Other

Posted 10 days ago

Job description

The Opportunity

The Clinical Data Management team at Amylyx Pharmaceuticals is seeking an Associate Director, Clinical Data Programmer. This individual will work collaboratively cross-functionally to provide hands-on data management support, programming support and technical leadership to develop, maintain, validate the clinical database, and run computer programs that access, visualize, and report clinical trial data, in accordance with various clinical plans, ICH guidelines, and applicable regulatory requirements. As an Associate Director of Clinical Data Programming, you will be required to program in the appropriate languages to create both textual and graphic displays that facilitate data cleaning and review.

Responsibilities

  • Lead the study-specific design, development, and validation of study clinical data capture systems, ensuring data integrity, CDISC compliance and CRO oversight.
  • Supports leading data management activities (i.e. DMP creation, CRF creation, edit checks creation, database lock), assisting with database setup, conduct and closeout phases.
  • Performs UAT of systems and ensures appropriate plans and documentation are in place.
  • Leads the development of SAS macros, data listings, summary tables and visualizations for supporting periodic and ad hoc data review.
  • Manages external vendor compliance and quality checks.
  • Supports Clinical Operations, Biostatistics and Data Management by providing data insight and solving technical data challenges.
  • Ensures databases adherences to SOPs, 21CRF Part 11, ICH-GCP and CDISC Standards (CDASH/SDTM)
  • Acts as a subject matter expert in leading technical initiatives and data management

Required Qualifications

  • Bachelor's degree or higher in Life Science or related discipline
  • 8+ years of experience in clinical data management
  • Extensive experience with clinical data systems (particularly Medidata Rave) and languages like SAS, R or Python
  • Proven experience in clinical trial programming and database management
  • Knowledge of Clinical Data Standards such as CDISC CDASH, and SDTM
  • Provide strong support to Data Management
  • Experience creating advanced interactive data visualizations from raw data using multi-languages and applications such as Using SAS, R, Python, RShiny, Power BI, Tableau, Spotfire etc.
  • Ability to manage multiple projects simultaneously, to manage conflicting priorities, and to be flexible when priorities change.
  • Excellent written and verbal communication skills and organizational and documentation skills.

Work Location and Conditions

  • At Amylyx, we proudly support remote work opportunities within the United States. However, due to business considerations related to health insurance coverage and state tax regulations, we are unable to hire employees who reside and/or work in certain states. Currently, we are not considering applicants from Alaska, Arizona, Hawaii, Michigan and Tennessee.
  • You will be expected to travel to our corporate location in Cambridge, MA several times a year and attend other company-related events as necessary and requested, which may include travel by air, driving or public transportation.
  • You must have access to work in setting that meets all requirements of the role (including privacy, reliable internet access, phone, ability to communicate via video conference, etc.) at your remote locatio

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