Senior Implementation Consultant - Pharmacovigilance Reporting (Remote)
Quick overview
Job description
The Role
What You'll Do
- Drive life sciences, customers, in the rapid configuration and implementation of Vault Workbench
- Act as Pharmacovigilance Reporting SME in global or complex implementations across all the different phases: workshop preparation and delivery, requirements gathering, gap analysis, configuration, validation, and customer training
- Deliver subject matter expertise on implementation methodology and best practices
- Collaborate with partners involved during the implementation
- Collaborate with internal and cross-team stakeholders and contribute to the Safety practice development
- Mentor project team and junior consultants
Requirements
- 5+ years of software consulting, data analysis, or technical implementation experience in the Life Sciences industry
- Hands-on experience developing pharmacovigilance reports and/or dashboards based on safety database data models
- Proven experience gathering pharmacovigilance reporting requirements from business stakeholders and translating them into technical specifications
- Solid understanding of relational database design, data structures, and report validation techniques
- Strong communication skills in English and experience leading customer-facing technical workshops
- Proven ability to deliver on quality, time, and budget
- A good team player with the ability to work autonomously in a fast-paced, high-growth environment
- Fast learner, ability to adapt, and to embrace changes
- Ability to travel upon business requirements
Nice to Have
- Direct experience with Veeva Vault applications, particularly Vault Safety or Safety Workbench
- Knowledge of Pharmacovigilance and drug safety processes, regulatory reporting, and aggregate/periodic reports (e.g., PSUR, PBRER, DSUR)
- Advanced proficiency in SQL for data extraction, transformation, and complex querying
- Experience with cloud data warehousing platforms (e.g., Snowflake, AWS Redshift) for advanced data analysis
- Direct experience with systems such as Oracle Argus, ARISg, and/or other drug safety applications
- Background working in a GxP-validated environment
Interviewing with Veeva
- 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, unless you have already completed it with Veeva previously.
- 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:
- A conversation with the hiring manager
- A practical case exercise
- A final conversation with our group's Senior Leader.
- Once all interviews are complete, the manager will be in touch with a final decision.
We value your time and believe in a transparent hiring process. Here is the process you can expect.
Compensation
- Total compensation: 90,000 - 150,000 EUR
- The total compensation range listed here has been provided to comply with local regulations and represents a potential total compensation range for this role. Please note that actual total compensation may vary within the range above or below, depending on experience and location. We look at compensation for each individual and base our offer on your unique qualifications, experience, and expected contributions. This position's total compensation may be composed of other types of compensation, such as variable bonus and/or stock bonus.
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#LI-MidSenior
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