Senior Consultant - Clinical Data Programming
Veeva Systems2 months ago
London, United KingdomSenior
Responsibilities
- Advise customers and clinical sites on trial design configuration, clinical data management, and Veeva best practices.
- Interpret clinical protocols and project specifications and lead database development activities according to project plans.
- Coordinate with sponsors, CROs, vendors, and clinical data providers to configure data transfers and integrations.
- Configure Vault CDMS forms, rules, study items, data imports, and SQL-based data-cleaning listings.
- Conduct user acceptance testing, manage feedback and issue resolution, and support study acceptance and go-live activities.
- Gather requirements, write technical specifications, identify risks, and communicate contingency plans to project management.
- Contribute to process, product, and best-practice initiatives while supporting developers and testers.
- Share data management challenges and end-user feedback with the Vault CDMS product team.
Requirements
- At least 5 years of experience with EDC clinical software and end-to-end clinical data management, including database design, data collection, analysis, query resolution, datasets, and statistical reporting.
- Solid understanding of clinical trial processes, particularly data collection and review.
- Programming experience with SAS, R, JSON, Python, or SQL and ability to learn new SQL-based languages.
- Life sciences industry experience in pharma, biotech, medical devices, CROs, or academic/public health, including project assessment, planning, development, training, and implementation.
- Experience in a customer-facing role, preferably in software professional services or consulting.
- Ability to work independently and collaboratively while meeting project timelines.
- Strong verbal, written, interpersonal, and presentation skills.
- Willingness to travel up to 10%, potentially including internationally.
- Familiarity with GCDMP, CDISC, SDTMIG, CDASH, or ADaM is preferred.
- Experience with clinical technologies or integrations such as IVRS, medical coding, eSource, CTMS, or eTMF is preferred.
- Experience with REST-based APIs, translating clinical protocols into software specifications, technical documentation, or Veeva applications is preferred.
- A degree in Life Sciences, Computer Science, or a related field is preferred.
Benefits
- Work-from-home or office flexibility as a Work Anywhere company; the role is open to remote candidates in the EU or UK.
- Full-time, permanent employment.
- Private health insurance.
- Flexible paid time off and local public holidays.
- Pension or retirement plan contributions.
- 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.