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Director for Regulatory Affairs IT with strong business understanding

Are you a born leader and can you successfully lead a well functional department with skilled employees? Do you have solid understanding of the pharmaceutical business processes and value streams? Do you think your knowledge of IT technologies are at top level?

Then we may have just the right job for you, where your decision will influence systems used across the organisation and be part of strategic decisions.

About the department
You will be responsible for the Regulatory Affairs (RA) IT department. The department is overall responsible for driving and executing the IT strategy for RA, and are responsible for IT projects (upgrades/replacements) with reach and impact across Novo Nordisk including Regulatory Affairs. Furthermore, you will be responsible for a team responsible for development and maintenance of smaller applications.

The department consist of 10 employees including a team leader for the team developing/maintaining smaller applications (RA IT Operations). It is the department’s responsibility to represent the Line of Business (LoB) and make sure that value is created in the IT solutions applied. You will be expected to make an impact by always striving for further improving our business and systems.

Global Regulatory Operations is a Corporate Vice President (CVP) area consisting of ~180 employees in Denmark and India. The CVP area is beyond IT responsible for Regulatory operational activities from labelling development and management, publishing activities, support in Clinical Trail Applications and Project Management.

The position
As Director of Regulatory Affairs IT, your main task is to govern and set a strategic direction to the department, where one of the big challenges is strategic decisions related to upgrading/replacing the IT platform, with comprehensive impact on the business arears. You give emphasis to employee management and focus on boosting collaboration and knowledge sharing within the team. Further, you effectively manage department budget and play a key role in contract negotiation and vendor management. Above all, you ensure that all the resources are in place to execute the IT strategy for Regulatory Affairs.

Similarly, you are trusted to align and manage IT project portfolio. Across the department, you ensure proper management and reporting of data and thereby, help monitor performance. You excellently manage high level stakeholders and ensure proper project communication. Eventually, you ensure proper follow-up plans and deliverables.

You are well aware of the latest technology developments, and monitor new external requirements and trends within your area. As a result, you successfully support the department in improving existing processes and implementing new technology.

Notably, you get a chance to represent the company and department in various forums and conferences. Likewise, you will also be member of different committees and groups critical to department projects.

Qualifications
You are an experienced leader with proven track record of creating business results. Additionally, you have strong people skills and are able to coach and motivate employees to deliver their best. You hold a Master degree in science, IT or have an equivalent educational background with at least 10 years of project management or management experience.

As a person, you possess integrity and a strong professional attitude. Your proactive, structured and dynamic approach enables you to deliver quality business results. Equally, you are dependable and are always ready to take risks.

Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us change lives for the better. 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 Maria Boese at +45 3079 6584.

Deadline
22 April 2018.


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