CONNECT Trial Manager Specialist
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Søborg
- Clinical Development and Medical
- Søborg
Connect Trial Manager Specialist
If you are ready to take part in what will be a corner stone in the digitalizing of Novo Nordisk, then we have the job for you! We can offer you the possibility to cooperate with highly experienced project managers, process experts and interact with stakeholders across the organisation. This is an important task - and we do it all in an agile and effective way!
About the department
You will be part of the Clinical Operations Office, a department which supports Global and Headquarter Clinical Operations with system support and development, training, solutions, information sharing, develops and drive innovation in the Clinical Operations area in Novo Nordisk. You will also be part of a dedicated team of 17 people supporting and continuously developing the CONNECT system, which is Novo Nordisk’s site-facing document exchange and training portal. CONNECT is a system in constant change and growth, which will continue to embrace new processes, to the benefit of both site staff and Novo Nordisk staff globally. CONNECT is a GCP-compliant system built on the most modern technology in the market.
The job
You will join a global skilled team consisting of technical, process- and business-oriented people, located primarily in India and Denmark, and with the collaboration of temporary resources from the CMR CDCs.
The Process and Compliance Specialist will, in collaboration with the CONNECT team, lead new features and improvements into the CONNECT platform, and thereby improve standardization and optimization of business processes and oversight.
You will be working agile in securing alignment between requests and wishes from line of business and the prioritized activities, which will be essential to ensure a successful implementation. You will need to balance the demands of the business here and now, while at the same time ensure our longer-term ambition is fulfilled. You will have a huge impact on utilising the full potential of a cloud-based IT system for clinical trial management. Many internal and external stakeholders will rely on your business understanding and your ability to combine business needs with an IT platform.
Some of your key activities will among others be:
- Provide expert knowledge of all phases of trial conduct processes
- Provide expert knowledge on documentation needed for site staff training
- Determine business requirements for new processes or functionalities
- Analyse requirements and work closely with the process and IT to implement prioritised activities
- Drive operational roll-out, support and communication to end-users
- Function as an advisor on CONNECT procedures and processes within the department and within trial management globally
- Be an ambassador for the CONNECT system usage and business value created
- Ensure simplicity and quality is built into solutions and processes
In your role, you will work closely with project managers and process experts to understand the needs of the business, as well as with colleagues in Global IT who will handle the IT development.
Qualifications
We are looking for a positive and solution-oriented candidate with an interest in business processes and IT system development.
Preferably you have 5-8+ years of experience within trial management, audits and inspections and well-founded in GCP and other external requirements. You have an analytical mindset, and you are able to work independently as well as being a strong decision maker. You are used to work in an environment where change is a constant.
You must be open to work in ways that are different from what you are used to and be comfortable with challenging our current status quo and comfortable in taking hard decisions even when the full picture is not clear.
We expect that you are structured and able to ensure overview. You are comfortable with challenging and advising stakeholders and you can present complex matters in a clear and precise manner. Above all, you are proactive, have a strong drive and a desire to create real impact for the business.
Working at Novo Nordisk
At Novo Nordisk, your skills, dedication and ambition help us 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.
Contact
For further information, please contact Birgitte Claudius on +45 3079 9668.
Deadline
12th of December 2020
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 chronic 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.
Information og data
Denne ledige stilling har jobtypen "Produktspecialist", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 12.11.2020, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Produktspecialist
- Søborg
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