senior consultant - safety - life sciences

As a Safety Consultant, you will be responsible for understanding our customers’ Quality needs and business processes, providing expert guidance, discussing application changes, translating requirements into solution design, and configuring document and data management systems (e.g. Veeva Vault) for managing Drug Safety information across the organization.  

You will support a dedicated group of customers to help them transition on their digital transformation journey.   

Your key responsibilities 

• Assist customers in implementing best practices within implementation / post-implementation programs aimed at ensuring their overall success.  

• Stay informed about best practices in the Pharmacovigilance field and offer actionable recommendations.  

• Technical abilities with willingness to “roll up your sleeves” to design solutions and configure the changes that meet customer needs.  

• Ability to collaborate and communicate with diverse stakeholders, including customer business and IT staff, to understand their requirements. 

• Establish trusted relationships with customer stakeholders. 

• Assist in the development and dissemination of thought leadership materials. 

Skills and attributes for success 

• Bachelor’s or Master’s degree in Management Information Systems, Computer Science, Life Sciences, or related fields. 

• 3+ years of consulting experience in configuring, supporting, or implementing software solutions. 

• Proven experience in a customer-facing role, managing expectations, facilitating difficult conversations, and delivering presentations or demos. 

• Strong background in Life Sciences with a particular interest in the Drug Safety domain. 

• Solid understanding of technologies used in Pharmacovigilance, particularly Veeva Vault applications (e.g. SafetyDocs, Safety, Workbench, Signal), and how PV consulting services can leverage and support these technologies. 

• Excellent verbal and written communication skills in English.  

• Ability to travel as required by the business.  

Ideally, you’ll also have 

• Direct experience with Argus and/or other drug safety applications. 

• Knowledge of computer systems validation requirements (following a GxP system development lifecycle). 

• Good grasp of the business capabilities and drivers behind digital technology in health and life sciences, as well as the market forces and trends influencing industry changes. 

• Proficiency in additional European languages. 

What we look for 

 We seek motivated, trustworthy professionals with strong communication skills and an analytical mindset. You thrive in high-performing teams, embrace challenges, and question the status quo. Curiosity, adaptability, and confidence to share ideas are essential. If you combine technical expertise with creativity, attention to detail, and a commitment to delivering exceptional quality while mentoring and collaborating, you’ll excel in our dynamic, multinational environment.