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How much do medidata rave specialist jobs pay per hour?

As of Sep 13, 2026, the average hourly pay for medidata rave specialist in the United States is $24.95, according to ZipRecruiter salary data. Most workers in this role earn between $18.27 and $28.85 per hour, depending on experience, location, and employer.

What is a Medidata Rave Specialist?

A Medidata Rave Specialist is a professional who manages and supports clinical data using the Medidata Rave electronic data capture (EDC) system. They are responsible for designing, configuring, and maintaining study databases, ensuring accurate data entry, and troubleshooting issues within the platform. These specialists often collaborate with clinical research teams to ensure compliance with regulatory standards and data integrity throughout clinical trials. Their expertise is crucial for the smooth operation of clinical studies that use Medidata Rave for data collection and management.

What are the key skills and qualifications needed to thrive as a Medidata Rave Specialist?

To thrive as a Medidata Rave Specialist, you need expertise in clinical data management, electronic data capture (EDC) systems, and a background in life sciences or related fields. Familiarity with Medidata Rave EDC software, database design, and often certification in Medidata Rave or relevant EDC platforms is typically required. Strong problem-solving, attention to detail, and effective communication skills help specialists collaborate with cross-functional teams and ensure data integrity. These skills are crucial for ensuring high-quality clinical trial data, regulatory compliance, and efficient study operations.

What are some common challenges faced by Medidata Rave Specialists when supporting clinical trial data management?

Medidata Rave Specialists often encounter challenges such as managing complex study protocols within the system, ensuring data accuracy, and troubleshooting technical issues that arise during study setup and ongoing data collection. They must collaborate closely with clinical data managers, study teams, and IT departments to resolve data discrepancies and maintain compliance with regulatory standards. Staying updated with frequent platform updates and adapting to varying sponsor requirements are also part of the role’s dynamic environment.

What are popular job titles related to Medidata Rave Specialist jobs?

For Medidata Rave Specialist jobs, the most frequently searched job titles are:

Oncology Clinical Research RN in Stamford, CT

Stamford, CT • On-site

Vivian Health
Recruiting and Staffing Services • 51 - 200 employees
Learn more about Vivian Healthexternal

Other

Re-posted 9 days ago

Job description

RN Clinical Research

Location Detail: 4185 Black Rock Turnpike (10596)

Shift Detail: Monday-Friday

Work where every moment matters.

Every day, more than 40,000 Hartford HealthCare colleagues come to work with one thing in common: Pride in what we do, knowing every moment matters here. We invite you to become part of Connecticut’s most comprehensive healthcare network.

The Hartford HealthCare Cancer Institute focuses on offering our cancer patients an unparalleled network of coordinated services– all under one roof. Our system of care includes a truly integrated team with the most talented, experienced, and compassionate caregivers and physicians, backed by the latest cutting-edge technology.

The Oncology Clinical Research Nurse (RN) of Cancer Clinical Research Office (CCRO) is an integral member of the research team. In compliance with all regulatory, institutional and departmental requirements, performs patient screening, data collection and data entry for research protocols, databases and projects within Hartford Healthcare Cancer Institute, and ensures the data quality and integrity for each clinical trial.
• Coordinate and facilitate the appropriate conduct of clinical research trials in oncology which may be supported by the NCI, industry, cooperative groups or HHC system alliances.
• Coordinate and conduct the operation of clinical trials as per GCP and ICH guidelines including participant recruitment; informed consent; continuous monitoring of protocol for compliance and patient safety; source document review; data entry; sponsor monitoring.
• Interact/collaborate with all physicians, other members of the health care team and participants/families across the system in a manner that supports the conduct of clinical trials.
• Required to attend the respective system-wide Disease Management Team meetings and present the clinical trials to potential investigators.
• Collaborate with and support other clinical trial staff across the system to ensure highest quality clinical research activities.
• Document relevant data collections into various sponsor electronic data capture systems and complete data entry within protocol timelines.
• Prepare study calendars and materials; maintain participant tracking logs and screening/enrollment logs.
• Assist regulatory staff with study regulatory reporting requirements and IRB policies for protocol deviations, safety reporting and continuing reviews.
• Assist research account specialist of CCRO with clinical trial billing in the resolution of related queries.
• Assist/coordinate preparation for internal and external audits.
• Handle all confidential information appropriately.

Qualifications
Requirements:
• Bachelor’s degree Nursing
• Minimum of 2-3 years of relevant clinical research experience.
• Demonstrated clinical competency with patient related measurements and with a high degree of accuracy with respect to documentation and data collection.
• Ability to work with spreadsheets (such as Excel), familiarity with databases (ex: Medidata, RAVE, IRIS, NSABP, GOG, RTOG etc.) and querying.
• Experience with Microsoft Access, Excel and electronic data capture systems.
• Experience in preparing and completing Case Report Forms (CRF’s), eligibility checklist and other relevant documentation protocols.
• Excellent interpersonal skills are required for working with the study participants and working as a member of a highly integrated team.
• Ability to travel between clinical sites, whenever required.

We take great care of careers.

With locations around the state, Hartford HealthCare offers exciting opportunities for career development and growth. Here, you are part of an organization on the cutting edge – helping to bring new technologies, breakthrough treatments and community education to countless men, women and children. We know that a thriving organization starts with thriving employees-- we provide a competitive benefits program designed to ensure work/life balance. Every moment matters. And this is your moment.

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