Mgr, Database Management Systems
$84K - $211K/yr
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 ...
Mgr, Database Management Systems
$84K - $211K/yr
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 ...
Provide mentoring, coaching, and escalation support to more junior personnel or contract staff, as ... Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards ...
Provide mentoring, coaching, and escalation support to more junior personnel or contract staff, as ... Medidata RAVE Custom Functions experience REQUIRED * C# programming experience REQUIRED * Standards ...
Biotech Specialist - AI Trainer
Houston, TX · On-site +1
$1.1K - $1.4K/wk
Contract Compensation: $1,150-$1,450 per completed task Location: Remote Role Responsibilities * Build a realistic digital workspace using tools like Medidata Rave , Oracle Clinical One ...
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Biotech Specialist - AI Trainer
Houston, TX · On-site +1
$1.1K - $1.4K/wk
Contract Compensation: $1,150-$1,450 per completed task Location: Remote Role Responsibilities * Build a realistic digital workspace using tools like Medidata Rave , Oracle Clinical One ...
Clinical Site Manager
Fort Worth, TX · On-site
Supports budget and contract negotiation with investigational sites, as applicable, at their ... Medidata RAVE preferred Clinical Trial Management System Experience required - Medidata CTMS ...
Clinical Site Manager
Fort Worth, TX · On-site
Supports budget and contract negotiation with investigational sites, as applicable, at their ... Medidata RAVE preferred Clinical Trial Management System Experience required - Medidata CTMS ...
Senior DevOps Engineer (US REMOTE)
Allen, TX · Remote
$140K - $170K/yr
Department Overview The Rave organization within Motorola Solutions is responsible for SaaS ... Government Contract Mandates and access to sensitive public safety data. * Experience with ...
Senior DevOps Engineer (US REMOTE)
Allen, TX · Remote
$140K - $170K/yr
Department Overview The Rave organization within Motorola Solutions is responsible for SaaS ... Government Contract Mandates and access to sensitive public safety data. * Experience with ...
Content Moderator - Austin
Austin, TX · On-site
$25K - $50K/mo
Leveraging our holistic portfolio of capabilities in consulting, design, engineering, and ... Update own availability in the RAVE system to ensure productivity of the process * Record, track ...
Content Moderator - Austin
Austin, TX · On-site
$25K - $50K/mo
Leveraging our holistic portfolio of capabilities in consulting, design, engineering, and ... Update own availability in the RAVE system to ensure productivity of the process * Record, track ...
Contract Medidata Rave Programmer information
What is a Contract Medidata Rave Programmer?
A Contract Medidata Rave Programmer is an information technology specialist hired on a temporary or project basis to design, configure, and maintain clinical trial databases using Medidata Rave, a leading electronic data capture (EDC) system in the pharmaceutical and biotechnology industries. Their responsibilities typically include creating electronic Case Report Forms (eCRFs), managing edit checks, programming custom data exports, and supporting data validation activities. These programmers collaborate closely with data managers, clinical teams, and statisticians to ensure that clinical data is accurately captured and compliant with regulatory standards.
What are the key skills and qualifications needed to thrive as a Contract Medidata Rave Programmer, and why are they important?
To thrive as a Contract Medidata Rave Programmer, you need expertise in clinical data management, EDC systems, and programming languages such as SQL or SAS, typically backed by a degree in life sciences or computer science. Proficiency with Medidata Rave, eCRF design, and understanding of CDISC standards are essential, along with relevant certifications like Medidata Rave Certified Professional. Attention to detail, analytical thinking, and effective communication are crucial soft skills for collaborating with cross-functional teams and ensuring data quality. These skills and qualifications are vital for building reliable clinical databases and supporting accurate data capture in regulated clinical trials.
How does a Contract Medidata Rave Programmer typically collaborate with clinical data management and biostatistics teams during a study?
As a Contract Medidata Rave Programmer, you will regularly interface with clinical data managers and biostatisticians to ensure that electronic data capture (EDC) systems meet protocol specifications and study requirements. You’ll participate in requirements gathering, review case report forms (CRFs), and address data validation needs, often through meetings and collaborative platforms. Effective communication and responsiveness are crucial, as you may need to troubleshoot issues, implement mid-study changes, or clarify data logic to support study timelines. This collaborative environment helps ensure high-quality data collection and smooth study execution.
What is the difference between Contract Medidata Rave Programmer vs Clinical Data Coordinator?
| Aspect | Contract Medidata Rave Programmer | Clinical Data Coordinator |
|---|---|---|
| Required Credentials | Bachelor's in Life Sciences, Clinical Research, or related field; experience with Medidata Rave | Bachelor's in Nursing, Life Sciences, or related; familiarity with clinical data management |
| Work Environment | Contract-based, primarily remote or on-site at clinical trial sites or CROs | Typically on-site at clinical research sites or hospitals, coordinating data collection |
| Employer & Industry Usage | Pharmaceutical companies, CROs, clinical research organizations | Hospitals, research institutions, pharmaceutical companies |
The Contract Medidata Rave Programmer focuses on configuring and maintaining electronic data capture systems using Medidata Rave, while the Clinical Data Coordinator manages data collection and quality at clinical sites. Both roles require knowledge of clinical data processes but differ in technical versus operational focus.
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What job categories do people searching Contract Medidata Rave Programmer jobs in Texas look for? The top searched job categories for Contract Medidata Rave Programmer jobs in Texas are:
What cities in Texas are hiring for Contract Medidata Rave Programmer jobs? Cities in Texas with the most Contract Medidata Rave Programmer job openings:
IQVIA rating
8.1
Based on 53 frontline employees who took The Breakroom Quiz
53rd of 208 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 athttps://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.
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