2402 Clinical Research Associate

Adecco A/S recruiting on behalf of Anecova in Copenhagen.
On behalf of Anecova, Adecco Medical and Science search for the best CRA interim employee – perhaps you’re already working as a freelance CRA at the moment.
Anecova is a life science company focused on the development and commercialization of new technologies in the field of Assisted Reproductive Technologies (ART). Our goal is to improve the overall quality of care in ART by enabling the use of more physiologic and natural processes.
The first Anecova product aims to restore the fertilization and early development of the embryo to the natural environment of the maternal womb. This technology enables the embryos to start their life in close communication with the maternal environment. This is expected to increase the number of high-quality embryos and improve the success rate of the assisted reproductive cycle.
The preliminary results are encouraging. We are therefore undertaking further clinical evaluation, in close collaboration with international experts in the field, with the goal of improving the experience of assisted reproduction for patients around the world.
Anecova are currently recruiting for a Clinical Research Associate (CRA) m/f on temporally basic from March to August 2010. The job is a part time job app. 15-20 hours pr. week (with the possibility for extension) home based office. The main investigation area is located primary close to Copenhagen.
Purpose for the job:
Coordinate execution of clinical trials in close collaboration and under the supervisor of the clinical research Project Manager.
Responsibilities and tasks:

• Key contact for our clinical partners, ensuring a good cooperation with them
• Management of investigator/investigational site. This includes investigational product specific knowledge (training, development of tools, handling assisting implementation and building experience)
• Ensure that the study runs timely and in line with local guidelines and the inclusion/exclusion criteria of the study
• Report progress of the study to headquarters (Switzerland) in a weekly basis.
• Monitoring of the study to ensure its run in compliance with Good Clinical Practice (GCP/ICH), MedDev, ISO 14155 and Clinical Development SOPs and Anecova’s QA system
• Archiving of study documentation and correspondence
• Participation in relevant project team(s), if appropriate

Requirements:
Clinical Research Associates require a life sciences degree or nursing qualification and experience of Phase II to IV trials and in depth knowledge of FDA and ICH GCP requirements.
Your questions and application:
For further question, sales manger Lotte Bonde at Adecco Medical and Science directly on mobile phone  +45 2368 7407  +45 2368 7407 or mail: lotte.bonde@adecco.dk
To make an application please send it by e-mail to lotte.bonde@adecco.dk.
We are looking forward to receiving your application.

                               
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