Are you motivated by driving innovation for the life-changing benefit of patients? Are you ready to help transform the treatment paradigm for a broad range of chronic diseases that currently rely on injection-based therapies? Then this is your moment. Apply now and join  Novo Nordisk. Together we can create life-changing innovation. Together we can make it happen.

 

The position

 

Performing monitoring according to plan, document actions and follow up on action plans Site selection visits incl. analysis of site logistics, site personnel performance/quality indicators and accountability for patient recruitment strategies Train and guide site staff in the protocol and trial procedures to minimise protocol deviations (PDs) Know and meet all local and company requirements with respect to safety reporting and train site staff in safety information handling and systems Proactive use of EDC and other data source systems for preparation and conduct of monitoring Source data verification and source data review activities as per trial needs Identify potential risks (by using Risk Indicator Report as well as other available tools and systems) and proactively take action to prevent or mitigate Ensure data cleaning cycle timelines are met in accordance with the Data Flow Plan Manage trial product requirements, incl. temperature deviations and training of site staff Ensure collaboration with and deliverables from vendors locally, if applicable Collection and management of essential documents Support the site in filing and archiving trial documentation in the Investigator Trial Master File (ITMF) Participation in Investigators Meetings to ensure relations with sites as well as active presentation as applicable

 

Qualifications

 

Bachelor or other degree in Life Sciences or equivalent, e.g. nursing, medical, or as identified in the respective Regions Ideally experience from a similar position in the pharmaceutical industry or Clinical Research Organisation (CRO). Other experience may also be relevant, e.g. as study staff at a clinical research site. Ability to build and maintain relationships with sites Responsible and accountable Excellent communication and negotiation skills High focus on delivery and quality Adequate English verbal and writing skills, e.g. enabling understanding of the protocol and study documents as well as writing monitoring reports Proven decision making and problem solving capabilities Ability to manage multiple priorities Team oriented personality with high degree of flexibility High degree of trustworthiness Act as an ambassador for NN values

 

 

Working at Novo Nordisk

 

At Novo Nordisk we recognise that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and the communities we operate in.

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. We are happy to discuss flexible working, depending on the role and subject to business needs.

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

 

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.