H. Lundbeck A/S

Lundbeck is a global pharmaceutical company specialized in psychiatric and neurological disorders. For more than 70 years, we have been at the forefront of research within neuroscience. Our key areas of focus are depression, schizophrenia, Parkinson's disease and Alzheimer's disease.

An estimated 700 million people worldwide are living with psychiatric and neurological disorders and far too many suffer due to inadequate treatment, discrimination, a reduced number of working days, early retirement and other unnecessary consequences. Every day, we strive for improved treatment and a better life for people living with psychiatric and neurological disorders – we call this Progress in Mind.

Read more at www.lundbeck.com/global/about-us/progress-in-mind.

Our approximately 5,000 employees in more than 50 countries are engaged in the entire value chain throughout research, development, production, marketing and sales. Our pipeline consists of several late-stage development programmes and our products are available in more than 100 countries. Our research centre is based in Denmark and our production facilities are located in Denmark, France and Italy. Lundbeck generated revenue of DKK 17.2 billion in 2017 (EUR 2.3 billion; USD 2.6 billion).

For additional information, we encourage you to visit our corporate site www.lundbeck.com and connect with us on Twitter at @Lundbeck and via our LinkedIn company page.


 

Senior International Study Manager


Are you passionate about working with clinical studies in an international environment, then we have an open position as Senior Study Manager in the Clinical Study Management department at Lundbeck.
Clinical Study Management is part of Lundbeck’s Research & Development organisation and the position is based at Lundbeck’s headquarters in Copenhagen.
Our department is responsible for managing interventional phase II-IV studies as well as observational studies at global level.

Your job
As International Study Manager, you are overall responsible for leading a global cross-functional study team consisting of participants from relevant functions within Development, proactive planning and execution of the study, as well as facilitating an excellent relationship with the investigational sites.
We conduct our studies in close collaboration with CROs and as an International Study Manager, you are responsible for the selection of the CRO, the day-to-day collaboration, and securing deliveries as per contract.
Travel days is to be expected.

We offer
We invite you to be part of Clinical Study Management where we share the common aspiration to become world’s best CNS Pharma within Study Design & Execution. We are focused, passionate and responsible towards our deliveries, colleagues and society.   We offer a positive and engaging working environment and we have a strong pipeline.

Our preferred candidate has the following profile:

Your professional qualifications

  • MSc or PhD level within medical, pharmaceutical, or biological sciences
  • more than 5 years of experience with managing or clinical studies, preferably in the pharmaceutical industry or within a Clinical Research Organization
  • experience in leading cross functional study teams
  • experience in managing CROs, including deliverables and budget oversight
  • international experience and a multicultural mind-set
  • fluent in written and oral English

Your personal qualifications

  • passionate about making a difference for patients suffering from psychiatric and neurological diseases
  • good at motivating others, achieving results together with and through others
  • excellent communication and coordination skills
  • pro-active, outgoing, goal-oriented, and dynamic
  • responsible and decisive
  • a team player and at the same time able to work independently
  • able to maintain a broad overview while keeping a sufficient level of detail

Further information
If you wish to know more about this job opportunity, please contact Manager, Trine Kolding at +45 30834428. We also recommend you to visit our website www.lundbeck.com.

Your application
Please apply for the job via link below. Applications must be received no later than 17 October 2018.

 
 

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Region:
Region Hovedstaden

Job type:
Permanent

Working hours:
Full-time

Working days:
Day

Location:
Copenhagen

[ Send application ]

Contacts:
Trine Kolding
Mobile: +45 30834428

Company homepage:
http://www.lundbeck.com