Senior Consultant - Clinical Data Programming
Veeva Systemsover 1 year ago
Base Salary
$80k - $200k/yr
Responsibilities
- Advise customers and clinical sites on configuring clinical studies to meet trial goals and maximize the benefits of Veeva CDMS.
- Review clinical protocols and project specifications, applying clinical data management and Veeva best practices.
- Drive database development activities and coordinate with sponsors, CROs, vendors, and clinical data providers.
- Configure Veeva Vault CDMS forms, rules, study items, data transfers, and Veeva DQS data imports.
- Develop SQL-based listings for customer data-cleaning requirements.
- Conduct remote or on-site user acceptance testing, coordinate feedback, resolve issues, and support study acceptance.
- Gather requirements and create specifications for integrations and go-live activities.
- Communicate risks and contingency plans, support regulatory and procedural compliance, and contribute to product and best-practice initiatives.
- Support developers and testers, participate in Vault CDMS product discussions, and train and mentor customer and internal teams.
Requirements
- 5+ years of experience with EDC clinical software and end-to-end clinical data management activities such as database design, data collection, analysis, query resolution, datasets, and statistical reporting.
- Working knowledge of clinical trial processes related to data collection and review.
- Programming experience with SAS, R, JSON, Python, and SQL, with the ability to learn SQL-based languages.
- Life sciences and clinical trial process expertise across design, documentation, data collection, planning, development, training, and customer implementation.
- Experience in customer-facing software professional services or consulting is preferred.
- Ability to work independently and collaboratively in a fast-moving environment while meeting project timelines.
- Excellent verbal, written, interpersonal, and presentation skills.
- Ability to travel up to 10%, potentially including internationally.
- Preferred qualifications include knowledge of GCDMP, CDISC, SDTMIG, CDASH, and ADaM standards; experience with clinical technology integrations and REST-based APIs; Veeva application experience; and a degree in life science, computer science, or a related field.
Benefits
- Remote, work-anywhere arrangement with no stated office 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.