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Medidata Rave Jobs (NOW HIRING)

IQVIA, Inc.

Mgr, Database Management Systems

Durham, NC · On-site

$84K - $211K/yr

Build and maintain Medidata Rave global library objects, including eCRFs, edit checks, and CRF Completion Guidelines. * Develop SAS programs for edit checks, data imports, listings, custom reports ...

MapLight Therapeutics

Clinical Data Manager

Burlington, MA · On-site

$145K - $160K/yr

Oversee Medidata Rave electronic data capture (EDC) system setup, configuration, user management, coding and data extracts. * Perform data cleaning, discrepancy management, SAE and vendor integration ...

Veristat

... e., Medidata Rave, Oracle InForm/ Central Designer, Veeva, DataLabs, Medrio. 4 years' experience leading eCRF Design/Development/ Maintenance projects and activities without support of a senior ...

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How much do medidata rave jobs pay per hour?

As of Jul 13, 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 job?

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 88% Full Time, 2% Part Time, and 10% Contract. Highlights an 79% In-person, 3% Hybrid, and 18% Remote job distribution, with an average salary of $126,558 per year, or $60.8 per hour.
Mgr, Database Management Systems

Mgr, Database Management Systems

IQVIA, Inc.

Durham, NC • On-site

$84K - $211K/yr

Full-time

Posted 8 days ago

IQVIA rating

8.1

Company rating: 8.1 out of 10

Based on 53 frontline employees who took The Breakroom Quiz

55th of 210 rated it services

Job description

Manager, Database Management Systems
Job Summary
Seeking an experienced clinical data professional to lead database management and clinical data standards activities supporting global clinical trials. This role will serve as a subject matter expert in clinical data standards, Medidata Rave global library development, and SAS programming, partnering with cross-functional teams to ensure high-quality, standardized clinical data collection and reporting.
Key Responsibilities
  • Lead development and maintenance of global clinical data standards, including CDISC-compliant operational data mappings and SDTM standards.
  • Build and maintain Medidata Rave global library objects, including eCRFs, edit checks, and CRF Completion Guidelines.
  • Develop SAS programs for edit checks, data imports, listings, custom reports, and clinical data validation.
  • Create and manage clinical datasets from raw data using Base SAS, Advanced SAS, Macros, PROC SQL, and SAS ODS.
  • Support CRF design, annotated CRFs, data mapping specifications, and define.xml requirements.
  • Collaborate with Clinical Data Management, Clinical Operations, EDC Programming, vendors, and CRO partners to ensure consistent standards implementation.
  • Drive process improvements, support governance committees, and provide mentorship to junior team members.
  • Ensure compliance with CDISC standards, GCP, ICH guidelines, and regulatory requirements.

Required Qualifications
  • Strong clinical domain knowledge with a solid understanding of clinical trial phases.
  • Prior work experience must be within the clinical research, pharmaceutical, biotechnology, healthcare, or CRO industry.
  • Hands-on experience programming Edit Check Listings using SAS.
  • Experience with Data Import Programming using SAS.
  • Experience utilizing SAS Output Delivery System (ODS) to generate reports in RTF, PDF, and HTML formats.
  • Experience reading raw data files, creating data structures, handling missing values, troubleshooting programming errors, and managing clinical data.
  • Experience appending and concatenating SAS datasets.
  • Proficiency developing reports using PROC PRINT, PROC FREQ, PROC MEANS, PROC TRANSPOSE, and PROC SQL.
  • Strong programming experience with SAS Macros and SQL.
  • Experience creating SAS datasets from raw clinical data, including status and efficacy datasets.
  • Ability to develop project-specific macros and formats, load client data from external platforms, and prepare datasets for client delivery.
  • Experience creating clinical listings and custom reports based on business requirements.
  • Knowledge of Vendor Import Programming.
  • Strong technical expertise in Base SAS, Advanced SAS, SAS Macros, SAS SQL, and SAS Grid.
  • Ability to develop code using Base SAS programs, SAS procedures, and standardized macros.
  • Excellent written and verbal communication skills.

Preferred Qualifications
  • Experience with CDASH and ADaM standards.
  • Extensive Medidata Rave global library development experience.
  • Knowledge of MedDRA, WHODrug, annotated CRFs, and data mapping specifications.
  • Experience with Veeva, Medrio, Oracle Clinical, TrialGrid, or similar EDC systems.
  • Demonstrated ability to lead cross-functional initiatives in a global clinical development environment.

IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com
IQVIA is proud to be an equal opportunity employer. All qualified applicants will receive consideration for employment without regard to race, color, religion, sex, sexual orientation, gender identity, national origin, disability, status as a protected veteran, or any other status protected by applicable law. https://jobs.iqvia.com/eoe
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
The potential base pay range for this role, when annualized, is $84,600.00 - $211,600.00. The actual base pay offered may vary based on a number of factors including job-related qualifications such as knowledge, skills, education, and experience; location; and/or schedule (full or part-time). Dependent on the position offered, incentive plans, bonuses, and/or other forms of compensation may be offered, in addition to a range of health and welfare and/or other benefits.

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About IQVIA

Sourced by ZipRecruiter

At IQVIA, we are passionate about helping customers and partners improve results and patient outcomes. Everything we do contributes to this vision for creating a healthier world. In today’s healthcare environment, it’s not only about how much data, information, and technology you have at your fingertips – it’s what you do with it. IQVIA is focused on making intelligent connections for customers across the entire healthcare ecosystem to help you drive healthcare forward. Whether that means partnering with novel technology companies to boost patient engagement, leveraging AI & machine learning to accelerate results, or using decentralized trials to reach the right patients wherever they are – we are always looking for smarter ways to move you forward.

Industry

Health care and social assistance

Company size

10,000+ Employees

Headquarters location

Durham, NC, US

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