Experience with at least one clinical EDC platform, such as Medidata Rave, REDCap, Veeva Vault ... Experience with Git, Azure DevOps, or similar version-control tools and controlled release and ...
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Experience with at least one clinical EDC platform, such as Medidata Rave, REDCap, Veeva Vault ... Experience with Git, Azure DevOps, or similar version-control tools and controlled release and ...
Veeva Developer information
Does Veeva Systems pay well?
Veeva Developer roles typically offer competitive salaries that reflect industry standards for software development and cloud-based solutions. Compensation can vary based on experience, location, and certifications, but generally, Veeva Developers are well-paid within the biotech and pharmaceutical sectors. Benefits often include opportunities for skill development with tools like Veeva Vault and CRM platforms.
Does Veeva offer training or development programs?
Veeva offers training and development programs for Veeva Developers, including online courses, certifications, and onboarding sessions to enhance skills in Veeva Vault and related tools. These programs help developers stay current with platform updates and industry best practices.
What is the difference between Veeva Developer vs Veeva Administrator?
| Aspect | Veeva Developer | Veeva Administrator |
|---|---|---|
| Primary Role | Develops and customizes Veeva Vault applications and modules | Manages and maintains Veeva Vault systems, user access, and configurations |
| Required Skills | Veeva Vault development, programming, API integration | Veeva Vault administration, user management, workflow setup |
| Certifications | Veeva Certified Developer | Veeva Certified Administrator |
| Work Environment | Technical teams, software development projects | Operational teams, system management |
While both roles work within the Veeva ecosystem, Veeva Developers focus on building and customizing applications, whereas Veeva Administrators handle system maintenance and user management. Understanding these differences helps organizations assign the right skills to each role.
What is a Veeva Developer?
A Veeva Developer is an IT professional who specializes in designing, developing, and maintaining applications on the Veeva platform, which is widely used in the life sciences industry for managing content, customer data, and regulatory processes. They work with Veeva products such as Vault, CRM, and QualityDocs, customizing solutions to meet business needs. Veeva Developers use programming skills, configuration tools, and integration techniques to enable companies to optimize their workflows and ensure compliance with industry regulations.
What are the key skills and qualifications needed to thrive as a Veeva Developer, and why are they important?
To thrive as a Veeva Developer, you need a solid background in software development, knowledge of Veeva Vault products, and experience with life sciences data management, often supported by a degree in computer science or a related field. Familiarity with Veeva Vault, Vault API, Java, SQL, and certifications such as Veeva Vault Platform Developer are highly valuable. Strong problem-solving skills, attention to detail, and effective communication set top performers apart in this role. These competencies ensure efficient implementation, customization, and support of Veeva solutions, driving compliance and productivity in regulated industries.
How much does Veeva sales development program pay?
Veeva sales development programs typically offer internships or entry-level roles with salaries ranging from $15 to $25 per hour or around $30,000 to $50,000 annually, depending on location and experience. Compensation may include benefits and opportunities for skill development in cloud-based software and pharmaceutical industry sales.
How hard is a Veeva interview?
The Veeva Developer interview typically involves technical questions related to Veeva Vault, programming skills, and understanding of cloud-based applications. Candidates may also be tested on their knowledge of data management, system configuration, and problem-solving abilities. Preparation with relevant certifications and hands-on experience can improve success rates.
What are some common challenges Veeva Developers face when integrating Veeva Vault with other enterprise systems?
Veeva Developers often encounter challenges related to data synchronization, API limitations, and maintaining data integrity when integrating Veeva Vault with other systems like ERP or CRM platforms. Each system may have different data models and security protocols, requiring careful mapping and robust testing to ensure seamless communication. Additionally, staying updated with Veeva's frequent platform updates and ensuring compatibility with external tools can require ongoing effort and collaboration with cross-functional teams.
What are popular job titles related to Veeva Developer jobs in Arkansas? For Veeva Developer jobs in Arkansas, the most frequently searched job titles are:
What job categories do people searching Veeva Developer jobs in Arkansas look for? The top searched job categories for Veeva Developer jobs in Arkansas are:
What cities in Arkansas are hiring for Veeva Developer jobs? Cities in Arkansas with the most Veeva Developer job openings:
Full-time
Medical, Dental, Vision, Life, Retirement, PTO
Posted 23 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.
About Arkana Laboratories
Sourced by ZipRecruiter
Industry
Outpatient health care
Company size
51 - 200 Employees
Headquarters location
Little Rock, AR, US
Year founded
2001