Senior Pharmacovigilance Technology Professional

SO PV Technology

Søborg, Denmark

Do you want to play a key role in ensuring the highest patient safety standards while supporting critical pharmacovigilance systems at Novo Nordisk? Are you motivated by working at the intersection of safety operations, technology and global collaboration? If so, this could be your next career step.

Your new role

As a Senior Pharmacovigilance Technology Professional, within Safety Operations, you will work alongside your colleagues to bridge end users and IT, drive the ongoing daily business administration and support continuous improvement of the global patient safety database - Veeva Safety, enabling high‑quality daily case processing and timely submission of Individual Case Safety Reports (ICSRs).

In addition, you will collaborate closely with trial data management to enable successful trial setup and execution in Veeva Safety, acting as a key interface between business, IT and global stakeholders.

Key responsibilities include:

• Evaluate and translate business and regulatory requirements into Veeva Safety business administrator changes, including for example maintaining picklists, products, clinical trials, submission rules, and related system setup.
• Collaborate with global trial management for trial enablement in the safety database, review protocols and eCRFs, and secure user acceptance testing for safety forms and integrations.
• Partner with clinical trial teams and stakeholders to optimize technical integration between Veeva Safety and Veeva EDC.
• Implement safety database updates by working closely with Enterprise IT and stakeholders, managing change requests, testing, and end-user support. Assist with gateway implementation and frequent system releases.
• Participate in cross-organizational projects and working groups, update SOPs, manage deviations, and support audits and inspections.

In this role, you will have the opportunity to both work independently and in collaboration with a team of highly skilled, committed and enthusiastic colleagues. Taking ownership, engaging with diverse stakeholders and proactively driving actions will be essential parts of your day‑to‑day work.

Your skills and qualifications

To succeed in this role, you have:

• Master’s degree in science, pharmaceutical or health science
• Several years of experience within the drug safety / pharmacovigilance area, including hands on experience working with safety databases and/or EDC systems from a business administrator perspective
• Experience as a Subject Matter Expert in large, cross-functional and cross-organizational projects

• Solid experience with safety data elements and the ability to translate regulatory requirements, focusing on drug development and lifecycle activities
• Ability to communicate in fluent English (both written and spoken)

On a personal level you:

• Bring a proactive, solution-oriented mindset, with the ability to navigate change and adapt quickly
• Demonstrate strong stakeholder management skills, engaging effectively across all organizational levels and communicating with clarity and impact
• Apply an enterprise mindset and thrive in a multicultural environment undergoing continuous development
• Combine strong analytical and organizational skills with structured execution

Your new department

You will join Safety Operations PV Technology, a department within Global Patient Safety. The department has global responsibility for the Veeva Safety business administration responsibilities and continuous improvement of Novo Nordisk’s global safety database. You will be part of an international team of 15 highly engaged colleagues and work closely across geographies and functions to ensure patient safety and regulatory compliance.

Working at Novo Nordisk

Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with determination, constant curiosity and a commitment to finding better ways forward. For over 100 years, this dedication has driven us to build a company focused on lasting change for long-term health. One where diverse thinking, shared purpose and mutual respect come together to create extraordinary results. When you join us, you're not just starting a job – you're becoming part of a story that spans generations.

What we offer

There is, of course, more on offer here than the uniqueness of our culture and the extraordinary results we produce. Being part of a global healthcare company means opportunities to learn and develop are all around us, while our benefits are designed with your career and life stage in mind.

Salary:  For this role, the Annual Base Salary ranges from 651,000.00 to 956,900.00 DKK, corresponding to the level of the position.

The placement within the salary range will be assessed during the recruitment process based on the candidate’s skills, competencies, knowledge, and relevant experience.

Incentives and Benefits: The salary package may include short-term and/or long-term incentives as well as other employee benefits based on position level, location, functional area and relevant market benchmarks.

Learn more about our Reward Philosophy here.

Deadline:
25 May 2026
Please note that we will screen applications and interview candidates on an ongoing basis, so please apply at the earliest.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants.

At Novo Nordisk, we're not chasing quick fixes – we're creating lasting change for long-term health. For over 100 years, we've been driven by a single purpose: to defeat serious chronic diseases and help millions of people live healthier lives. This dedication fuels our constant curiosity and inspires us to push the boundaries of what's possible in healthcare. We embrace diverse perspectives, seek out bold ideas, and build partnerships rooted in shared purpose. Together, we're making healthcare more accessible, treating and preventing diseases, and pioneering solutions that create change spanning generations. When you join us, you become part of something bigger – a legacy of impact that reaches far beyond today.