Clinical Trial Coordinator

Clinical Trial Coordinator

August 21, 2011
WE ARE LOOKING FOR

We are looking for a Clinical Trial Coordinator with the desire to participate in conducting

clinical investigations with medical devices in Europe. If you have a proven “can do”

attitude and you like working in an international environment, you might be interested

in the position.

JOB PROFILE

In Clinical Research, we are responsible for coordinating clinical studies together with

our US-based counterpart. As part of a transatlantic clinical project team, you will get

the opportunity to participate in managing the European part of the investigations

from start to end. We have investigations within the SBUs Peripheral Intervention and

Endoscopy. You must be willing and able to travel.

Your responsibilities as a Clinical Trial Coordinator will be to:

Help submitting clinical documents to Competent Authorities and Ethics Committees to obtain approvalsTrain sites in Electronic Data Capturing SystemHelp provide clinical study agreements, carry out safety reporting, coordinate investigational devices, create notes to files, and reimburse the sitesEstablish close working relationships with physicians, their research staffs, and outside consultants through exceptional communication on a regular basisAssist the Clinical Project Leader in conducting meetings with investigative sites, physicians, and consultantsArchive study related documents in coordination with team membersRespond promptly and appropriately to study issues raised by investigative sites, sponsors, monitors, and consultants.JOB PROFILE

We are looking for a colleague with good interpersonal skills. It is obvious that you

work independently with your own responsibilities and thrive on an international

dynamic environment.

As a Clinical Trial Coordinator, we also expect you to have the following qualifications:

A Nursing degree or a Masters degree in Health, Life Science, or Biomedical EngineeringWorking knowledge of ISO 14155, MDD, FDA, and other regulatory requirementsPreferably experience in conducting clinical investigationsExperience in using Electronic Data Capturing SystemExcellent communication skills and fluency in verbal and written EnglishWE OFFER

Cook Medical has a healthy company culture with a strong common set of values, and

responsible, competent and professional staff is our most important resource. We have

a flat organizational structure with the focus on open dialogue. Qualities such as determination,

loyalty and humor are highly appreciated.

The staff of Cook Medical helps to uphold the company’s philosophy of developing

innovative medical solutions to raise the quality of patient treatment worldwide - we

make a difference!

ADDITIONAL INFORMATION

For further information about the position, please contact Susanne Holm Faarbæk,

Clinical Manager, on +45 56 86 86 86 or e-mail Susanne.Faarbaek@cookmedical.com

APPLICATION LETTER

Please send your application letter and CV (both in English) to Anne-Mette Vangkilde,

HR Generalist, by August, 10.

You may also e-mail your application to job@cook-wce.com .

COMPANY PROFILE

Cook Medical is a leader in researching, developing and manufacturing medical technologies that improve quality of life for people around the world. To provide our customers with the best possible support, we have nine strategic business units (SBUs) that each specializes in a particular segment of medicine. Products are manufactured on three continents and are distributed to 135 countries. In Denmark, we currently employ around 650 people.

William Cook Europe, Sandet 6, 4632 Bjæverskov, Denmark


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