Senior Implementation Consultant – Pharmacovigilance Reporting
New
V
Veeva SystemsLife sciences
Opportunities are available across the UK/Germany for this role; this is a 'work anywhere' positionFull-TimeSenior
Salary not disclosed
Apply NowOpens the employer's application page
Job Details
- Languages
- Strong communication skills in English
- Experience
- 5+ years of software consulting, data analysis, or technical implementation experience in the Life Sciences industry
- Required Skills
- SQLSnowflake
Requirements
- Have 5+ years of software consulting, data analysis, or technical implementation experience in the Life Sciences industry.
- Have hands-on experience developing pharmacovigilance reports and/or dashboards based on safety database data models.
- Have experience gathering pharmacovigilance reporting requirements from business stakeholders and translating them into technical specifications.
- Have a solid understanding of relational database design, data structures, and report validation techniques.
- Have strong communication skills in English and experience leading customer-facing technical workshops.
- Be able to deliver on quality, time, and budget.
- Be able to travel as business requirements require.
- Veeva Vault application experience, particularly Vault Safety or Safety Workbench, is advantageous.
- Knowledge of pharmacovigilance and drug safety processes, regulatory reporting, and aggregate or periodic reports such as PSUR, PBRER, and DSUR is advantageous.
- Advanced SQL proficiency and experience with cloud data warehousing platforms such as Snowflake or AWS Redshift are advantageous.
- Experience with Oracle Argus, ARISg, or other drug safety applications is advantageous.
- Experience working in a GxP-validated environment is advantageous.
Responsibilities
- Lead the design, development, and deployment of pharmacovigilance reporting and data analytics solutions using Vault Workbench.
- Configure and implement Vault Workbench for life sciences customers.
- Act as the Pharmacovigilance Reporting subject matter expert across implementation phases, including workshop preparation and delivery, requirements gathering, gap analysis, configuration, validation, and customer training.
- Translate pharmacovigilance data needs into reports, dashboards, extracts, and technical specifications.
- Deliver implementation methodology and best-practice expertise.
- Collaborate with implementation partners and internal cross-team stakeholders.
- Contribute to Safety practice development.
- Mentor project team members and junior consultants.
View Full Description & ApplyYou'll be redirected to the employer's site
