Senior Consultant Bardi

Senior Consultant
Bardi
Emilia Romagna, Bardi

col-wideJob Description:

Understanding customers' data management needs and challenges, offer guidance and direction to ensure that the clinical trial is designed with the deliverable in view.

Responsible for authoring all specification documents used by team members and configuring the study design Importante Azienda the development phase of the project.

What You'll Do

Configure Veeva products Importante Azienda development,

Support the requirements gathering and specification creation process for all study integrations,

Lead customer requirement and testing sessions,

Notify project management of project risks and develop contingency plans as necessary,

Ensure customer success from beginning to end of the project life cycle,

Assure process compliance with all regulatory and Veeva procedural requirements,

Deliver post go-live configuration changes.

**Requirements**:

5+ years experience in end-to-end data management related activities in EDC (database design, data collection, data analysis, query resolution, datasets, statistical reporting),

Strong understanding of data management standards and guidelines (GCDMP, CDISC, SDTMIG, CDASH),

Experience in interpreting clinical protocols and translating requirements into software specifications including writing and reviewing technical documentation,

Experience in a customer-facing role, preferably with a software professional services organization or consulting background is preferred,

Proven ability to work independently in a dynamic, fast-moving environment, but also as part of a team,

Proven track record of meeting project timelines/deliverables and attention to detail, process, deadlines, and quality results,

Excellent verbal and written communication, interpersonal, and presentation skills,

4-year college degree required,

Ability to travel 25-30% (may include international).

Nice to Have

Hands-on data management experience,

Experience working with system integrators for IVRS, medical coding, eSource, CTMS, eTMF, and other clinical technologies,

Experience with defining data standards and libraries,

Life Science, computer science or related degree,

SaaS/Cloud experience in the delivery of clinical trials,

Experience with training for clinical sites and at investigator meetings,

Consulting experience,

Fluency in one or more of the following languages:

German, French, Spanish, Italian.

Perks & Benefits

Allocations for continuous learning & development

Health & wellness programs