Senior Consultant - Clinical Data Programming
Veeva Systemsover 2 years ago
Base Salary
$80k - $200k/yr
Responsibilities
- Advise customers and clinical sites on clinical trial design and configuration in Veeva CDMS.
- Consult with customers on clinical protocols, requirements, specifications, implementation plans, and industry best practices.
- Drive clinical database development activities with sponsors, CROs, and external vendors.
- Configure forms, rules, study items, custom SQL-based listings, and Veeva DQS data ingestions.
- Coordinate clinical data transfers from providers such as central laboratories, ECG, eCOA, and IRT systems.
- Conduct user acceptance testing, coordinate feedback, resolve issues, and support study acceptance.
- Support requirements gathering, integrations, documentation, training, and go-live activities.
- Communicate project risks and contingency plans while ensuring regulatory and procedural compliance.
- Mentor customers and internal teams and support developers and testers throughout the project lifecycle.
- Contribute clinical data management feedback to Vault CDMS product and best-practice initiatives.
Requirements
- 5+ years of experience with EDC clinical software and end-to-end clinical data management activities.
- Working knowledge of clinical trial processes involving data collection and review.
- Programming experience with SAS, R, JSON, Python, SQL, or comparable languages, with ability to learn SQL-based languages.
- Life sciences and clinical trial expertise across design, documentation, data collection, planning, development, training, and customer implementation.
- Experience in a customer-facing software professional services or consulting role.
- Ability to work independently and collaboratively while meeting project timelines and quality standards.
- Strong verbal, written, interpersonal, and presentation skills.
- Ability to travel up to 10%, potentially including international travel.
- Preferred experience with data management standards including GCDMP, CDISC, SDTMIG, CDASH, and ADaM.
- Preferred experience integrating IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies.
- Preferred REST-based API integration and programming experience.
- Preferred experience interpreting clinical protocols, translating requirements into software specifications, and writing or reviewing technical documentation.
- Experience with Veeva applications and a Life Science, Computer Science, or related degree are preferred.
Benefits
- Remote, work-anywhere arrangement with no work location requirement when near an airport and able to meet travel requirements.
- Full-time permanent employment with up to 10% travel.
- Medical, dental, vision, and basic life insurance.
- Flexible paid time off and company-paid holidays.
- Retirement programs.
- 1% charitable giving program.
About Veeva Systems
Veeva Systems builds cloud software and data products for life sciences, including Veeva CRM and the Veeva Vault suite for clinical, regulatory, and quality operations. It sells subscriptions and services to biopharma and related companies to manage R&D, compliance, and commercial workflows. Founded in 2007 and headquartered in Pleasanton, California, Veeva is publicly traded on the NYSE and has operated as a Public Benefit Corporation since 2021.