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 delivers the industry cloud for life sciences with software, AI, data, and business consulting. Committed to innovation, product excellence, and customer success, Veeva serves more than 1,500 customers, ranging from the world’s largest biopharmaceutical companies to emerging biotechs. As a Public Benefit Corporation, Veeva is committed to balancing the interests of all stakeholders, including customers, employees, shareholders, and the industries it serves. For more information, visit veeva.com. Correspondence to new applicants and existing candidates will only come from an official @veeva.com email address.