Pharmacovigilance professional with strong drive and project management skills

• Clinical Development and Medical
• Bagsværd

Are you ready to apply your pharmacovigilance knowledge together with your personal skills, dedication and ambition to be part of a team of highly qualified and committed people at Novo Nordisk? Are you looking for a role where you can be part of a truly global workplace, where passion and engagement are met with opportunities for professional development? If you find this exciting and inspiring, you may be our new Pharmacovigilance Compliance Professional.

About the department

The position is located in Global Safety Compliance, which is part of the QPPV Office under Global Safety. Global Safety is globally responsible for handling of adverse events, monitoring product safety, customer complaints and potential recalls in Novo Nordisk.

The primary responsibilities of the Global Safety Compliance department are ICSR Compliance Tracking, Safety Data Exchange Agreements, Pharmacovigilance System Master File, Regulatory Surveillance, coordination of PV Audits and Inspections, support to HQ functions and affiliates, including compliance advice and support regarding handling of safety in Patient Support Programmes, Market Research Programmes and Digital Health initiatives. We are 10 colleagues with different professional background ensuring support to the Qualified Person for Pharmacovigilance in Novo Nordisk, Global Safety and affiliates worldwide.

The position

As Pharmacovigilance Compliance Professional, you will be involved in maintenance of our pharmacovigilance processes by providing advice and support, contribute to improvement efforts and initiatives, and participate in audits and inspections. You will be expected to keep an eye on any quality or compliance concerns that require escalation to management. Furthermore, you will be responsible for providing training to internal employees on procedural matters, and ensure coherence between requirements and internal operating procedures and guidelines in collaboration with other colleagues in the department.

Qualifications

You hold a Master’s Degree in biomedical sciences. A solid knowledge of pharmacovigilance is essential, preferably from a similar position within the pharmaceutical industry. Project management experience is a clear advantage. You are fluent in both written and spoken English and possess excellent communication skills.

Furthermore, you have strong skills in maintaining complex information whilst still working with the details of the information in a structured approach. As a person, you are open-minded and enthusiastic and you should have excellent collaboration skills, a high degree of flexibility and be used to delivering according to targets. IT flair and analytical skills are highly desirable. We expect you to work independently and have the ability to drive a variety of tasks.

Working at Novo Nordisk

At Novo Nordisk, your skills, dedication and ambition help us change lives for the better for patients around the world. As their needs evolve, so does our challenge to find better and more innovative ways to improve their quality of life. In exchange, we offer you an opportunity to work with extraordinary talent and benefit from a range of possibilities for professional and personal development.

Contact

For further information, please contact Eirik Quamme Bergan at +4530793513

Deadline

10 September 2020.

Please note that applications will be assessed on an ongoing basis and therefore the advert may close before the recruitment process is completed if we have proceeded with candidates to the screening or interview phase.

Millions rely on us
To work for Novo Nordisk you will need the skills, dedication and ambition to change lives for the better for millions of patients living with diabetes and other chronical diseases. In exchange, we offer the chance to be part of a truly global workplace, where passion and engagement are met with opportunities for professional and personal development.