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Medidata Rave Jobs (NOW HIRING)

Medidata Solutions

Senior Data Scientist

New York, NY · On-site

$114K - $153K/yr

Medidata is powering smarter treatments and healthier people through digital solutions to support ... The AI features developed will power modern clinical trial study design and study conduct with Rave ...

TechData Service Company LLC

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

Irvine, CA · Remote

$40 - $45/hr

Experience with Medidata Rave is required Preferred Qualifications: * Local candidates are preferred, with a hybrid work schedule of 3 days on-site and 2 days remote/WFH. * Qualified remote ...

Join Parachute

Head of Clinical & Registry Programs

Austin, TX · On-site

$79K - $108K/yr

Hands-on with at least one EDC/registry platform (REDCap, Castor, Medidata Rave RWS, OpenClinica, Veeva CDMS). * Has built and negotiated site participation agreements and BAAs/DUAs at scale (10+ ...

Join Parachute

Head of Clinical & Registry Programs

Austin, TX · On-site +1

$79K - $108K/yr

Hands-on with at least one EDC/registry platform (REDCap, Castor, Medidata Rave RWS, OpenClinica, Veeva CDMS). * Has built and negotiated site participation agreements and BAAs/DUAs at scale (10+ ...

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How much do medidata rave jobs pay per hour?

As of Aug 6, 2026, the average hourly pay for medidata rave in the United States is $60.85, according to ZipRecruiter salary data. Most workers in this role earn between $50.96 and $69.23 per hour, depending on experience, location, and employer.

What is a Medidata Rave?

A Medidata Rave job typically involves working with Medidata Rave, a widely used electronic data capture (EDC) system in clinical trials. Professionals in this role manage study databases, design case report forms (CRFs), ensure data integrity, and support clinical research teams. Roles may include Rave Study Builder, Data Manager, or Clinical Programmer. Strong knowledge of clinical trial processes, database management, and SQL is often required.

What are the key skills and qualifications needed to thrive in the Medidata Rave position, and why are they important?

To thrive as a Medidata Rave specialist, you need a solid understanding of Electronic Data Capture (EDC) systems, clinical data management, and regulatory guidelines, typically supported by certifications in Medidata Rave or relevant clinical research fields. Proficiency with the Medidata Rave platform, user administration, and familiarity with tools such as SQL or other database management systems are highly valued. Strong attention to detail, communication, and problem-solving skills help professionals stand out in this role. These qualities ensure accurate data collection, regulatory compliance, and effective collaboration in complex clinical trial environments.

What are some common challenges faced by Medidata Rave specialists in clinical trials?

Medidata Rave specialists often encounter challenges such as ensuring data accuracy across multiple sites, managing complex study protocols, and troubleshooting technical issues within the platform. They are responsible for configuring case report forms, supporting site users, and maintaining regulatory compliance, which requires constant vigilance and adaptability. Collaboration with clinical research teams, sponsors, and IT staff is vital to address study-specific needs and resolve problems efficiently. These challenges make the role dynamic but also provide opportunities for continuous learning and professional growth.

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Medidata Rave jobs near you
Infographic showing various Medidata Rave job openings in the United States as of July 2026, with employment types broken down into 50% Full Time, and 50% Contract. Highlights an 100% In-person job distribution, with an average salary of $126,558 per year, or $60.8 per hour.

Clinical Trials Data Management Specialist

Arkana Laboratories

Little Rock, AR

Full-time

Re-posted 3 days ago

Job description

Who we are: At Arkana Laboratories, everyone has an important role to fill. Come join us and be a part of a team dedicated to making life better for those who need it most.

This place is packed with super-smart people who do their best work together. We work hard every day to advance our understanding of disease and provide world-class care to our patients in hopes of leaving our corner of the world a little better than we found it. While we are committed to improving the lives of thousands of patients, we never lose sight of the realization that they are the reason we get to create change in our field.

Built on generosity, teamwork, and the freedom to try new things, we take great pride in our work. Great ideas come from everywhere in this company and we celebrate each success and failure for the opportunity it gives us to keep reaching. For more than twenty years after our founder, Dr. Patrick Walker, wrote his goals on the back of a napkin, our people, culture, and values have remained strong.

Position Summary: We're looking for a Clinical Trials Data Management Specialist who can turn approved Data Transfer Agreements, database specifications, CRFs, and protocols into clean, validated Python scripts, and who takes real ownership over transfer readiness and data quality along the way. You'll dig into test and production transfer files, catch discrepancies before they become problems, and keep documentation audit and inspection ready every step of the way. You'll also flex into EDC QC and build support, helping confirm that what's collected lines up cleanly with what needs to be delivered.
What you'll do:
Data Transfer Scripting and Clinical Data Quality
  • Create, update, and validate Python-based scripts used for data extraction, transformation, QC checks, and sponsor-ready file generation.
  • Translate approved DTAs, database specifications, CRFs, protocols, scoring forms, and sponsor requirements into documented transfer logic and output rules.
  • Prepare and QC test and production transfer files using record counts, field-level checks, format checks, source-to-target review, reconciliation, and expected-value checks.
  • Review transfer requirements before scripting to identify required fields, mapping rules, visit naming, controlled terminology, date formatting, file structure, blinding considerations, and delivery dependencies.
  • Investigate transfer issues related to missing records, formatting problems, mapping gaps, value-range discrepancies, file structure, naming conventions, encoding, or sponsor feedback.
EDC QC, UAT, and Build Support
  • Perform QC of EDC builds, CRF configurations, edit checks, workflows, and data collection requirements against protocol and study-specific requirements.
  • Participate in study start-up scoping, UAT, amendment updates, and transfer-readiness discussions to help confirm EDC data collection aligns with downstream transfer needs.
Clinical Trials Team Partnership
  • Work closely with the CT Data & Project Lead and CT Data Specialist/EDC Builder to keep CRFs, raw exports, transformation logic, and sponsor deliverables aligned.
  • Participate in script review, peer review, and transfer-readiness discussions, and provide practical scripting guidance where appropriate.
  • QC data transfer or scripting-related tasks completed by team members and document findings, questions, and resolution steps.
  • Follow team documentation, validation, version-control, and change-tracking practices, including clear notes for script updates and releases.
You should have:
Required
  • 1-2 years of experience in clinical data, EDC systems, data QC, data transfer support, scripting, or another regulated data environment.
  • Working proficiency with Python or a comparable scripting language for data extraction, transformation, validation, and output-file generation.
  • Strong attention to detail and experience reviewing data across CRFs, exports, listings, specifications, source requirements, and final transfer outputs.
  • Ability to document assumptions, validation evidence, issue resolution, change history, and production-readiness decisions clearly.
Preferred
  • Experience with at least one clinical EDC platform, such as Medidata Rave, REDCap, Veeva Vault, Oracle Clinical, Inform, or a similar system.
  • Experience working with DTAs, database specifications, CRFs, data dictionaries, source-to-target mappings, or sponsor transfer requirements.
  • Experience with C#, Rave custom functions, edit check logic, or similar clinical system programming.
Strong Bonus
  • Hands-on Medidata Rave experience, especially Rave Architect, Designer, edit checks, UAT, or build-level support.
  • Familiarity with CDISC, CDASH, SDTM, controlled terminology, and sponsor-ready or regulatory-ready clinical datasets.
  • Experience with Git, Azure DevOps, or similar version-control tools and controlled release and change-tracking practices.
Education: Bachelor's degree preferred. Equivalent directly related experience may be considered in lieu of a degree.
This is a Monday-Friday 8:00AM-5:00PM onsite position at our main office in Little Rock, Arkansas.

What we offer: We know that health is more than doctor visits and life is more than work. We work hard at Arkana but in turn provide competitive salaries and generous benefit offerings.

Specifically, we offer the following benefits to full-time employees:

  • Competitive salary
  • Generous paid time off and Paid Holidays
  • Minimal cost health insurance for you and affordable options for your family
  • 401(k) with immediate eligibility and match
  • Company-paid life insurance
  • Company-paid long term disability coverage
  • Affordable vision and dental plans
  • Flexible Spending Account or Health Savings Account availability
  • Wellness plan and complimentary yoga classes
  • Monthly in-office massages and employer-sponsored lunches

Please see Careers for further information.