Clinical Affairs Monitor
CellaVision AB / Apotekarjobb / Lund
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hela Sverige CellaVision is an innovative, global medical technology company that develops and sells its own leading systems for routine analysis of blood and other body fluids in health care services. The analyses often constitute important reference data for fast and correct diagnosis of illnesses such as viral and bacterial infections and cancers. CellaVision's products rationalize manual laboratory work, and secure and support effective workflows and skills development within and between hospitals. The company has leading-edge expertise in image analysis, artificial intelligence and automated microscopy. In 2015 sales were SEK 239 million. Sales continue to increase, with a growth target of at least 15 % per year over an economic cycle. CellaVision's registered office is in Lund, Sweden and the company has subsidiaries in the USA, Canada, Japan, Republic of Korea and Dubai. The share is listed on the OMX Stockholm, Small Cap list. Read more at
www.cellavision.com CellaVision is strengthening the team with a Clinical Affairs Monitor. The main duty for the position will be to facilitate studies in both non-clinical and clinical phases, as well as the pre- and post-market studies. You will also be an active part in interacting with internal experts/sponsors in product related projects. The organizational place for this position is in the Quality department and you will report to the Clinical Affairs Manager.
Responsibilities
Plan, coordinate, manage and monitor clinical studies and make sure that they are in compliance with all applicable regulations and company procedures.
Assist the Clinical Affairs Manager in managing clinical studies & in preparing clinical protocols and other documents needed for clinical studies.
Establish and maintain professional relationships (in person, by phone and/or email) with hospital laboratories and distributors as necessary to support clinical studies.
Process data from clinical studies.
Interact with all departments at CellaVision as well as directly interact with investigators and study staff.
Requirements
Academic degree BSc in Science, preferably biomedical laboratory science.
A good organisational skill to be able to support the planning, monitoring and reporting of clinical studies related to medical device, preferably IVD or experience of working in a controlled laboratory environment.
Experience within hematology is desirable.
Qualifications
We believe that you like to work independently, prioritizing your work tasks in a sufficient manner and you have an outgoing, energetic and result oriented hands-on personality.
Furthermore, you possess the ability to work with several projects and activities at the same time. Your computer skills are excellent and high in common Microsoft Office Environment.
Travelling requirements
You will have approximately 20 to 40 traveling days yearly.
Contact and application
For more information about this position please contact recruiting manager Karin Hannander, Clinical Affairs Manager, by e-mail:
karin.hannander@cellavision.com To apply for this position, please click "apply for this job" to forward your CV and cover letter, no later than March 17 2017.
Varaktighet, arbetstid
Heltid Anställningstid enligt överenskommelse
Publiceringsdatum2017-03-02Ersättning Lön enligt överenskommelse
Så ansöker duSista dag att ansöka är 2017-03-18
Klicka på denna länk för att göra din ansökanKontaktKarin Hannander
karin.hannander@cellavision.comFöretagCellaVision AB
AdressCellaVision AB
Mobilvägen 12
22362 Lund
KontorsadressMobilvägen 12, Lund
Jobbnummer 3350719
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