ZipRecruiter

Log In

1

Volunteer Clinical Programmer Medidata Rave Jobs

Medidata Solutions

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

  • Medical

  • Dental

  • Life

  • Retirement

  • PTO

The AI features developed will power modern clinical trial study design and study conduct with Rave ... Medidata believes that benefits should connect you to the support you need when it matters most and ...

Xencor

Sr. Director, Clinical Science (Autoimmune)

San Diego, CA · On-site

$84K - $115K/yr

  • Medical

  • Retirement

More than 20 XmAb drug candidates engineered with our technology are in clinical development, and ... MS Office Suite, Visio, GraphPad Prism, Spotfire, Medidata RAVE, Inform etc. * Ability to work ...

previous page

Showing results 41-60

All JobsVolunteer Clinical Programmer Medidata Rave Jobs

Volunteer Clinical Programmer Medidata Rave information

See salary details

$24

$64

$102

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

As of Aug 16, 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?

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 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:

What states have the most Volunteer Clinical Programmer Medidata Rave jobs?

States with the most job openings for Volunteer Clinical Programmer Medidata Rave jobs include:

Volunteer Clinical Programmer Medidata Rave jobs near you

Senior Manager / Manager, Clinical Data Management

Kodiak Sciences Inc.

Palo Alto, CA

Full-time

Re-posted 18 days ago

Job description

Kodiak Sciences is a biopharmaceutical company committed to researching, developing, and commercializing transformative therapeutics to treat a broad spectrum of retinal diseases. We are focused on bringing new science to the design and manufacture of next-generation retinal medicines to prevent and treat the leading causes of blindness globally. This role is on-site at Kodiak's headquarters in Palo Alto, CA. 
 
We are seeking a dedicated and detail-oriented person to support data management activities for clinical trials. This role will contribute to database development, data quality oversight, and vendor coordination to ensure accurate, compliant, and submission-ready data. The ideal candidate will bring strong hands-on experience and a collaborative mindset, working closely with cross-functional teams to drive successful trial execution and regulatory submissions.
 
Responsibilities
  • Support the design, development, and validation of clinical trial databases and electronic Case Report Forms (eCRFs) at the study level.
  • Oversee data cleaning, query resolution, and delivery of high-quality datasets to support trial milestones and regulatory submissions.
  • Collaborate with external data management vendors to ensure timely and high-quality deliverables; track performance against project timelines and quality standards.
  • Participate in the preparation, review, and validation of submission-ready datasets for regulatory filings (e.g., NDA, BLA, MAA).
  • Ensure compliance with industry standards and regulations (GCP, FDA, EMA) and assist in audit and inspection readiness.
  • Coordinate with internal stakeholders including Clinical Operations, Biostatistics, Regulatory Affairs, and IT to ensure smooth data integration and reporting.
  • Contribute to the implementation and optimization of clinical data systems and tools (e.g., EDC, data review platforms).
Education / Qualifications
  • Bachelor’s degree in Life Sciences, Data Science, Computer Science, or a related field.
  • 10+ years of experience in clinical data management within the biotech, pharmaceutical, or CRO industry.
  • Experience managing study-level data management activities and working with external vendors.
  • Familiarity with clinical data systems (e.g., Medidata RAVE, Oracle Clinical, Veeva) and industry data standards (e.g., CDISC, SDTM).
  • Demonstrated experience supporting regulatory submissions is a plus.
  • Strong problem-solving, organizational, and communication skills.

Apply