Clinical Trial Application Coordinator in CTA Management
Denne stilling er desværre ikke længere ledig.
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Søborg
- Regulatory
- Søborg
1 Year temporary position, starting as soon as possible
Are you strong at planning, coordinating, problem solving and collaboration across an organisation? Do you have experience within clinical trial activities? Are you eager to drive operational clinical trial application (CTA) activities across the Novo Nordisk portfolio of projects and products? Then you might be the CTA Coordinator we are looking for in CTA Management.
About the department
The CTA Management department is a team of 9 motivated and engaged employees and is part of Submission & Labelling Management in Regulatory Affairs. It is a centralised unit responsible for coordination, planning and distribution of all CTA document packages submitted to Health Authorities and Ethics Committees worldwide.
CTA Management is a department in constant development and we are working closely with our stakeholders to continuously improve our processes to adapt and ensure compliance with the increasingly complex regulatory environment. We offer interesting and challenging assignments and good opportunities for continuous personal and professional development.
The position
You will have a central coordinating role in the planning, distribution and maintenance of worldwide CTAs across the entire Novo Nordisk portfolio of projects and products. In this role, you will facilitate cross-organisational collaboration and provide operational support as well as CTA local requirement expertise to our stakeholders in headquarters and affiliates.
As a CTA coordinator in CTA Management, you will also have the opportunity of being involved in continuous improvement activities and projects within the department and across the organisation for developing, optimising and standardising the Novo Nordisk CTA process.
Qualifications
You have a B.Sc. within natural sciences or other relevant background and preferably 2 years of experience working within Regulatory Affairs or Clinical Development. You have a quality mind-set and excellent overview, planning and coordination skills, and you enjoy working in a structured way in order to meet tight deadlines. You are motivated by taking the lead and have strong communication and presentation skills. Having a have a flair for IT systems and experience with MS Office applications. We also expect you to be fluent in written and spoken English.
On a personal level, you thrive in a busy environment and bring a positive can-do attitude to your work. You are outgoing, a strong team player and enjoy working in a diverse working environment with various stakeholders globally and across the organisation.
Contact
For further information, please contact Fi With Gjessø at +45 30777812.
Deadline
18 Nov 2020
Please note that we screen applications on a daily basis and invite candidates for interviews before deadline.
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 "Jurist", og befinder sig i kategorien "Økonomi og jura".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 17.11.2020, 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.
- Jurist
- Søborg
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