Senior Consultant - Clinical Data Programming

The Role

What You’ll Do

Act as a trusted advisor to customers and clinical sites, ensuring trial designs are configured to meet their goals, and providing training and mentorship along the way
Work with customers to interpret clinical protocol requirements and project specifications, applying industry and Veeva best practices
Lead database development activities per the project plan, coordinating with sponsor, CRO, and other vendor teams
Coordinate with clinical data providers (central labs, ECG, eCOA, IRT, etc.) to configure data transfers
Configure forms, rules, and other study items in Vault CDMS, and build custom SQL-based listings for customer data cleaning needs
Run on-site or remote user acceptance testing, managing feedback, issue resolution, and study acceptance
Support requirements gathering and specification writing for study integrations and go-live activities
Flag risks and contingency plans to project management to keep the project compliant with regulatory and Veeva procedures
Contribute to process, product, and best-practice initiatives, and support developers and testers throughout the project lifecycle
Share data management activities, challenges, and end-user feedback with the Vault CDMS product team
Configure and support data imports into Veeva DQS

Requirements

5+ years of experience with EDC clinical software, covering end-to-end data management (database design, data collection, data analysis, query resolution, datasets, statistical reporting)
Solid understanding of clinical trial processes, particularly around data collection and review
Programming experience in languages such as SAS, R, JSON, Python, or SQL, with the ability to pick up new SQL-based languages
Background in the life sciences industry (pharma, biotech, medical device, CRO, or academic/public health), with experience across project assessment, planning, development, training, and implementation
Experience in a customer-facing role, ideally within software professional services or consulting
Ability to work independently and collaboratively in a fast-paced, dynamic environment while meeting project timelines
Strong verbal and written communication, interpersonal, and presentation skills
Willingness to travel up to 10%, potentially including international travel

Nice to Have

Familiarity with data management standards (GCDMP, CDISC, SDTMIG, CDASH, ADaM)
Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, or similar clinical technologies
Experience integrating or programming with REST-based APIs
Experience translating clinical protocols into software specifications, including technical documentation
Experience with Veeva applications
Located near a major life sciences hub
Degree in Life Sciences, Computer Science, or a related field

Interviewing with Veeva

We value your time and believe in a transparent hiring process. Here is the process you can expect.

Follow the application process and submit your resume.

Within 3 days, you will receive a link to a personality assessment administered by a third party.

Once you complete the assessment, our team will review your full application package and follow up via email with our decision.

If moving to the interview stage, the process is as follows: 

1. A conversation with the hiring manager
2. A practical case exercise
3. A final conversation with our group's Senior Leader.

Once all interviews are complete, the manager will be in touch with a final decision. 

Perks & Benefits

Private health insurance
Flexible paid time off plus local public holidays
Pension / retirement plan contributions
1% charitable giving program

Employment type

Full-Time