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Senior International Trial Manager (Søborg, Denmark)

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Senior International Trial Manager

- Research & Development, Trial Manager
- Denmark - Søborg

Do you have extensive experience in driving global clinical trials and do you want to exert your influence by managing large global trials in rheumatoid arthritis or growth hormone disorders? Are you also prepared to embrace and tackle constant changes as part of your work each day? Then we may have just the right job for you.

About the department
Inflammation & Growth Hormone is the newest therapeutic area in Novo Nordisk. In Clinical Operations, Inflammation & Growth Hormone, we are now approx. 40 employees and we continue to grow as the pipeline matures. We are characterised by a world-class team spirit and quality mind-set, by our change readiness and an open, trust-based and creative working environment. We are responsible for the planning and implementation of clinical trial activities in accordance with the Clinical Development Plans in Inflammation and Growth Hormone, including trials in Rheumatoid Arthritis (RA), Crohn’s Disease (CD), Systemic Lupus Erythematous (SLE) and Growth Hormone Deficiency disorders. We collaborate internationally with other R&D units, with CROs and to a growing extent, with our Novo Nordisk affiliates.

The job
The job as Senior International Trial Manager demands that you are capable of directing and driving large global phase 2b/3 trials. You will be responsible for ensuring that project key deliverables are met in time, at a high quality and within budget. You will be a member of the international study group, for which you will plan and conduct team meetings that maximise information sharing, stakeholder engagement and decision making. This includes vendor management of CROs participating in the trial execution. You will participate in and contribute to relevant investigator and monitor meetings.

The job requires that you apply a structured and analytical approach during development of relevant trial documents such as trial protocol, informed consent, recruitment strategies, risk analysis plans, communication plans and trial budgets. You are detail-oriented, while able to maintain overview, digest complex data and evaluate the adequate level of quality.

You are expected to be able to identify better practices and create improvements and you will be able to chair cross-project/cross-functional tasks forces. You may act as trainer across projects and mentor new staff.

Qualifications
You hold an academic degree within the natural sciences or healthcare, and speak and write English fluently. You are a clear communicator and can inspire and motivate a team to deliver their best in an ever-changing environment. You have a strong knowledge of clinical trial planning and execution and a minimum of 5 years’ experience in managing large clinical trials.

You have a quality mind-set, communicate effectively and know how to prioritise between different tasks in a dynamic environment which requires a high degree of flexibility. You work independently while also being a dedicated team player. You have excellent cross-cultural awareness and like to contribute to multi-cultural project groups.

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.

You will be part of a successful, expanding company in which working is not just a way to make a living, but a way to make a difference.

Contact
For further information, please contact Louise Høyer at +45 3075 1535 or David Mollerup at +45 3079 9133.

Deadline
9 June 2013.

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