Event Adjudication professional (Maternity cover)

• Clinical Development & Medical
• Bagsværd

Are you knowledgeable within drug development and do you have experience with clinical trial conduct and operational project management? Do you want to cooperate with stakeholders across the organisation? Then we may have the right job for you. We are looking for an Event Adjudication Professional to join our Safety Operations (SO) Event Adjudication department for a maternity cover. The Event Adjudication department belongs to Safety Operations, one of the functional areas in Global Safety and the department is situated in Bagsværd.

About the department
The Event Adjudication department consists of 20 highly engaged team members from various academic backgrounds; who work in a fast-paced environment reflecting increasing demands from numerous long-term clinical trials and regulatory authority requirements. In an increasing number of trials, certain clinical adverse events are required to be adjudicated. Event adjudication is a process where an independent review board of medical specialists assesses the relevant events for fulfilment of pre-defined clinical criteria.

The position
As an Event Adjudication Professional you will be a driving factor between Safety Operations, different stakeholders in Global Development e.g. Medical & Science, Data Management & Trial Management and external service providers (CROs) dealing with event adjudication in selected clinical development projects. You will be involved in setting up and ensuring processes for event adjudication on clinical trials in close cooperation with the internal and external stakeholders. Project management, CRO oversight, on-going event tracking, process document preparation, and creating and communicating reports are examples of what this dynamic role comprises of. The role varies according to the life of a clinical trial with regard to pace and task type. Some of these tasks are data and database driven. The job may require some travel.

Qualifications
You hold a university degree (e.g. pharmacy, veterinary, biology) or equivalent. Knowledge of clinical development methodology is a prerequisite and experience in event adjudication, pharmacovigilance, Good Clinical Practice (GCP) and project management is an advantage. The job requires proficiency in English, in addition to high communication-, coordination and planning capacities and a strong quality mind-set. You are highly skilled in the Microsoft Office Package. You are proactive and like to work independently, as well as in a team. You have excellent cooperative skills and a high degree of flexibility. As a person you are open-minded, dynamic, and eager to learn new processes and have a positive attitude to challenges.

Working at Novo Nordisk
We offer an exciting job with lots of challenges among good colleagues in a positive working environment. At Novo Nordisk, we strive for excellence. As a world leader in diabetes care and a major player in haemostasis management, growth hormone therapy and hormone replacement therapy, we offer our employees opportunities for continuous growth.

Contact
For further information about the job please contact Ane Skou Elgaard at +45 3075 0958 or Kirsten Bang Rungby at +45 3079 6242.

Deadline
27 October 2019.

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.