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stillingsbetegnelse:
Medical Doctors to Medical & Science for Devices & Titration

jobbeskrivelse:

We are expanding and seeking two dedicated Medical Doctors with interest in medical devices and clinical development, who wishes to bring better treatments to people. Join us, and you will be working with highly talented and engaged colleagues striving passionately to create better treatments and care for patients suffering from a range of chronic diseases including diabetes, obesity, haemophilia, or growth hormone deficiency. 

Global Development is responsible for clinical development of new products based on proteins and peptides and their administration. We are involved from the early development phases to product introduction and throughout life cycle management. We manage clinical drug and device development worldwide, ensuring that processes meet uniform global standards, regulations and business ethics. We work in cross-organisational global project teams with focus on delivering viable products that make a difference to patients and ultimately benefit society.

 

About the department

Medical & Science Devices & Titration is part of Global Development and has medical responsibility for the drug delivery devices (e.g. pen-injectors and connectivity devices) and new technologies (including digital technologies) supporting development of new drugs as well as life cycle management of marketed products. The department is also responsible for treat-to-target in our clinical trials. We are a team of 9 experienced and ambitious Medical Doctors, each medically responsible for several development projects. 

Our organisation is project-centric. Internally we work in cross-functional teams, often at the interface between drug development and device development. Our key external stakeholders are the scientific and medical community, medical experts, and regulatory authorities.

 

The position

As Medical Doctor in Novo Nordisk (Medical Specialist) you will take on the role as the medical and scientific expert within the assigned medical device projects. Your tasks will include input to, and medical review of key documents related to conceptualisation, design and development of medical devices. You will assess the need for clinical trials, and establish clinical development programmes in a dynamic collaboration with Device Research & Development, Clinical Operations, Marketing, Regulatory Affairs, and other internal functions. This entails being involved from the initial idea for a project throughout development, testing in patients, submissions to health authorities, bringing the product to the market, and during the life cycle management phase. Furthermore, you will together with a cross-functional team be responsible for the clinical evaluation of medical devices, where all data supporting safety, effectiveness, and benefits is assessed using your clinical background to describe the context of the device, and your scientific background to identify and understand several data sources. 

You will be a driving factor in the cross-organisational implementation of clinical strategies, and have the medical responsibility during execution of the Product Development Plan. In addition, you will be responsible for providing high quality input for new submissions to health authorities as well as feedback to questions posed by health authorities worldwide. Finally, you will maintain and chair a cross-functional scientific board of internal and, if required, external research colleagues involved in the different phases of the product development. The job will require some travelling (approximately 5-30 days/year).

 

Qualifications

You must have a university degree as medical doctor and preferably knowledge within diabetes, obesity, haemostasis, growth hormone deficiency and/or medical device development including scientific training at PhD level or similar. Equally it is an advantage, but not a prerequisite, if you have clinical experience, experience within drug or medical device development, experience working with software as a medical device or experience in strategy planning from previous work in the pharmaceutical industry. 

You are an open-minded and dedicated team player, who thrives in a global cross organisational environment of continuous development, and focuses on completion, quality and results. The job requires proficiency in English, high communication-, coordination-, and planning capabilities, as well as flexibility and a keen sense of quality.

 

Working at Novo Nordisk
We are an organisation with many international employees and we welcome local as well as non-local applicants. We offer an inspiring and ambitious working environment, internal and external training, alongside the flexibility that allows you to influence your own working day. It is expected that you contribute with your own ideas as well as build upon the ideas of others. We believe that is what stimulates the ingenuity to develop the next generations of cutting-edge treatments.

At Novo Nordisk, your skills, dedication and ambition help us improve our patients’ lives. 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 additional information, please contact Thomas Sparre +45 3075 9160.
 

Deadline          

10 March 2019
 

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 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.

numberOfPosts: 1

jobCategoriesCodes_0: http://data.europa.eu/esco/isco/C2149

abstractJV_contact_0: Please apply using one of the specified channels

positionTypeCode: directhire

contractTypeCodes_0: fulltime

Arbejdsgiver Navn: Novo Nordisk A/S

source: DK-STAR