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Work From Home Clinical Programmer Medidata Rave Jobs

Atorus Research

Sr Medidata RAVE Programmer

Sr Medidata RAVE Programmer Remote from anywhere in the U.S. or Canada Contract/Corp to Corp JOB ... in clinical database design and deployment • Additional relevant work experience will be ...

EDETEK

Clinical Database Programmer

Good communication skills and ability to work with data management, clinical operations, programming, QA, vendors, and sponsor teams. Preferred Qualifications * Medidata Rave database build ...

TechData Service Company LLC

Be Seen First

Clinical Data Analyst II (LC18401-1)-Remote position

Irvine, CA · Remote

$40 - $45/hr

... Medidata Rave is required Preferred Qualifications: • Local candidates are preferred, with a ... and 2 days remote/WFH. • Qualified remote candidates within the U.S. will be considered.

Celerion

EDC Developer / Programmer

... Veeva Clinical Database (CDB) * Ensure secure and high-integrity database imports from vendor ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Celerion

EDC Developer / Programmer

OR · Remote

... Veeva Clinical Database (CDB) * Ensure secure and high-integrity database imports from vendor ... Veeva CDMS, Medidata RAVE, etc.) * Experience with Veeva EDC and Veeva CDB preferred * Proficient ...

Everest Clinical Research

Clinical Database Designer I

$50K - $90K/yr

... Work from Home policy. Key Accountabilities: * Design clinical database for new studies based on ... Medidata Rave, Clinical One, and/or other EDC systems. * Software programming experience relevant ...

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 ... Your work informs how leading labs train and evaluate the next generation of AI systems

IQVIA

Senior Data Team Lead (Remote)

Austin, TX · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

IQVIA

Senior Data Team Lead (Remote)

Myrtle Beach, SC · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

IQVIA

Senior Data Team Lead (Remote)

Dallas, TX · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

IQVIA

Senior Data Team Lead (Remote)

Las Vegas, NV · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

IQVIA

Senior Data Team Lead (Remote)

Charlotte, NC · Remote

$86K - $217K/yr

This is a remote/WFH position with all necessary equipment provided. What You'll Do * Lead data ... Expertise with Medidata Rave, Oracle InForm, or similar EDC systems. * Strong understanding of GCP ...

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All JobsClinical Programmer Medidata Rave JobsWork From Home Clinical Programmer Medidata Rave Jobs

Work From Home Clinical Programmer Medidata Rave information

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

As of Jul 27, 2026, the average hourly pay for work from home 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 Work From Home Clinical Programmer using Medidata Rave, and why are they important?

To thrive as a Work From Home Clinical Programmer specializing in Medidata Rave, you need a solid background in clinical data management, programming (such as SQL, SAS, or R), and a degree in life sciences or a related field. Familiarity with Medidata Rave EDC, CDISC standards (SDTM, CDASH), and certifications like Medidata Rave Certified Study Builder are often required. Strong attention to detail, problem-solving abilities, and effective remote communication are vital soft skills for excelling in this role. These competencies ensure accurate data capture, regulatory compliance, and seamless collaboration across globally distributed clinical research teams.

How does a work-from-home Clinical Programmer using Medidata Rave typically collaborate with study teams and resolve data management issues remotely?

As a remote Clinical Programmer specializing in Medidata Rave, you will frequently interact with data managers, clinical research associates, and biostatisticians through virtual meetings and collaboration tools. You'll be responsible for programming study databases, building and validating electronic case report forms (eCRFs), and troubleshooting data discrepancies. Effective communication and proactive problem-solving are key, as you may need to quickly address queries or implement changes based on feedback. Most organizations use platforms like Microsoft Teams, Slack, or email to facilitate real-time collaboration, ensuring that despite working remotely, you remain integrated with the wider study team.

What is a Work From Home Clinical Programmer Medidata Rave?

A Work From Home Clinical Programmer Medidata Rave is a professional who remotely designs, builds, and manages electronic data capture systems for clinical trials using Medidata Rave software. They are responsible for creating study databases, programming edit checks, and ensuring data integrity and regulatory compliance. These programmers work closely with clinical teams to support the collection, analysis, and reporting of clinical trial data, all while working from a remote location. Their expertise in Medidata Rave and clinical data management is essential for the successful execution of clinical studies.

What is the difference between Work From Home Clinical Programmer Medidata Rave vs Work From Home Clinical Data Coordinator?

AspectWork From Home Clinical Programmer Medidata RaveWork From Home Clinical Data Coordinator
Required CredentialsBachelor's in Life Sciences, Clinical Data Management, or related field; experience with Medidata RaveBachelor's in Life Sciences, Clinical Data Management; some roles may require certification
Work EnvironmentRemote, primarily using Medidata Rave for data entry and managementRemote or hybrid, managing data entry, cleaning, and query resolution
Employer & Industry UsagePharmaceuticals, CROs, biotech firms using Medidata RavePharmaceuticals, CROs, clinical research organizations

While both roles involve clinical data management, the Clinical Programmer focuses on configuring and programming data capture in Medidata Rave, whereas the Data Coordinator handles data entry, cleaning, and query resolution. Both roles are often remote and require similar educational backgrounds, but their specific responsibilities and tools differ.

What cities are hiring for Work From Home Clinical Programmer Medidata Rave jobs? Cities with the most Work From Home Clinical Programmer Medidata Rave job openings:
What states have the most Work From Home Clinical Programmer Medidata Rave jobs? States with the most job openings for Work From Home Clinical Programmer Medidata Rave jobs include:
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Work From Home Clinical Programmer Medidata Rave jobs near you
Infographic showing various Work From Home Clinical Programmer Medidata Rave job openings in the United States as of July 2026, with employment types broken down into 100% Full Time. Highlights an 100% Remote job distribution, with an average salary of $134,731 per year, or $64.8 per hour.

Sr Medidata RAVE Programmer

Atorus Research

Remote

Contractor

Posted 6 days ago

Job description

Sr Medidata RAVE Programmer
Remote from anywhere in the U.S. or Canada
Contract/Corp to Corp
JOB OVERVIEW
The Electronic Data Capture (EDC) Programmer is responsible for providing support in creating, deploying and maintaining clinical databases and provides EDC programming support to the study team in accordance with Atorus and/or sponsor standard operating procedures (SOPs), Good Clinical Practice (GCP), ICH Guidelines and sponsor requirements. The EDC Programmer also assists in technical support for data collection systems.
JOB RESPONSIBILITIES
• Perform study set up and program edit check programming as per the approved specifications with minimal guidance from the line manager or experienced colleagues
• Adhere to project timelines
• Participate in the design and maintenance of the clinical study database per the protocol and any amendments, SOPs, GCP and other regulatory requirements
• Review database specifications and Data Validation Specifications (DVS) and perform programming and configuration activities
• Assist in database release to production activities
• Provide programming or other support and assist CDM managers in daily technical operations. Respond to and solve technical oriented problems in a timely manner, as appropriate for the position. Assist data manager with status reports and listings as necessary
• Advise management on a regular basis on the status and any potential risks or concerns with ongoing projects to ensure timely resolution including any potential issues with resources
• Ensure awareness of project-specific quality and performance standards and ensure that these are adequately documented, communicated, and understood
• Participate in internal and external study team meetings, as required
• Participate in department meetings and initiatives
• Perform other duties as required by the department
QUALIFICATIONS AND EDUCATION REQUIREMENTS
• University/college degree (life science, pharmacy or related subject preferred), or certification in a related allied health profession from an appropriately accredited institution (e.g., nursing certification, medical or laboratory technology)
• 2-4years EDC Programming experience working in pharmaceutical, biotechnology or Contract Research Organization (CRO) preferred
• Course completion of an EDC system training
• Minimum 2-4 years of experience in clinical database design and deployment
• Additional relevant work experience will be considered in lieu of formal qualifications
• Broad knowledge of drug development processes
• Understanding of global clinical development budgets and relationship to productivity targets
• Knowledge of effective clinical data management practices
PREFERRED SKILLS
• Good organizational skills
• Good communication skills, verbal and written
• Detail oriented
• Good computer skills, including Microsoft Office and use of data management systems
• Good problem-solving skills
• Basic knowledge and understanding of EDC and other eTechnologies
• Flexible, team player
• Proven ability to organize and effectively prioritize workload and deliverables

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