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stillingsbetegnelse:
Clinical Compliance Coordinator with focus on quality and standardisation

jobbeskrivelse:

Global Development, Søborg, Denmark

Our growth is your opportunity

In Global Development, we take responsibility for new products based on proteins and peptides from early development phases to product introduction. We are responsible for managing clinical drug development worldwide, securing that the process lives up to uniform global standards, regulations and business ethics. We work in global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society. 

If you are motivated by supporting the standardisation, optimisation and quality of the Novo Nordisk Clinical Trial Standard Operating Procedures (SOPs), you may be our new Clinical Compliance Coordinator in Global Clinical Compliance, Global Development.
 

About the department

The area R&D Quality is divided into three departments. The open position is as a Clinical Compliance Coordinator for the Global Clinical & Research QMS department. The Global Clinical & Research QMS department is responsible for the Novo Nordisk clinical Quality Management System globally including optimising the processes and ensuring the mirroring of external requirements in the clinical SOPs. The department is specifically responsible for ensuring that NN SOPs can be globally implemented as well as our clinical QMS is maintained.

The job
Together with 14 colleagues, you will be responsible for ensuring that Novo Nordisk maintains one global clinical quality management system in compliance with GCP and other relevant external and internal requirements. You will be part of the team responsible for ensuring the administrative process for updating clinical trial Standard Operation Procedures (SOPs) in accordance with relevant schedules and requirements, and that the format of the documentation is in accordance with the required standards. You will participate in the planning and reporting of meetings for the group within Novo Nordisk responsible for maintaining Clinical Trial SOPs (The Clinical Trial SOP Council). 

Much of your responsibility will be performed independently, but it is essential that you are an excellent team player who is able to help build a strong network with your colleagues in the team as well as in the rest of headquarters and in affiliates.

Qualifications

You may have a bachelor’s degree in business language (English) or equivalent or English as native language, and experience from a highly structured administrative position. You have experience within the clinical area in the pharmaceutical industry and SOP update coordination. You are an experienced user of MS Office and motivated to master new IT systems. 

The ideal candidate will have a strong quality mindset and a high degree of initiative and independence. You are well structured with an eye for detail without loosing the overview. To be successful in this job you need to be both service-minded, and a positive and creative team player.

 

Contact

For further information, please contact Susanne Nørskov Jørgensen at phone: +45 3079 8151.    
 

Deadline

17-Mar-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.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2421

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR