[Date Prev][Date Next][Thread Prev][Thread Next][Date Index][Thread Index]

[AUDITORY] Open position - Advanced Bionics Clinical Research International



Dear list,

 

We have a new open position in the International Clinical Research Department at Advanced Bionics. The position is described below, and here is the link to apply!

 

https://jobs.sonova.com/s/VVkQNh

 

Please circulate within your networks!

 

Best regards

Laure Arnold

 

Who we are

In a life without sound, our work provides meaning. As a leading provider of innovative hearing care solutions, we are not just a company that makes products: we are a team on a mission to help people enjoy the delight of hearing. To enable a life without limitations, we – through our core business brands Phonak, Unitron, Hansaton, Advanced Bionics and AudioNova – develop, manufacture and distribute solutions that push the limits of technology and redefine the future of our industry.

Hannover, Germany

Regulatory Clinical Affairs Specialist (m/f/d) - Remote working possible (within Europe)

In Hanover, Germany, Advanced Bionics runs the European Research Center (ERC), founded in 2009. The ERC coordinates research and technology as well as regulatory clinical affairs activities in Europe. The ERC works in close cooperation with European clinics, technology providers and universities.

 

Our Offer for your Engagement:

  • Sonova and our brands offer very good perspectives and career opportunities
  • Atmosphere of mutual trust in a highly motivated team
  • Modern work environment and equipment
  • You help to improve the quality of life of millions of people with hearing loss
  • Opportunity to share your ideas with us

 

Main tasks and responsibilities:

  • Ensure compliance with Medical Device Regulation (MDR) requirements to obtain and sustain product approval by TÜV: Post-Market Clinical Follow-up and support of Clinical Evaluation documentation
  • Ensure departmental processes comply to regulations and standards (e.g. EU MDR, ISO 14155)
  • Support and conduct pre- and post- market clinical studies to obtain and sustain product approval by TÜV

 

Your profile:

  • Master in a scientific domain such as biomedical engineering, physics, audiology
  • Training on regulatory clinical requirements: in depth knowledge of EU MDR and ISO 14155
  • Minimum 2 years of experience in regulatory clinical affairs for medical devices ideally for class III devices or in the auditory implant domain
  • Willingness to travel internationally (20%)
  • English: excellent written/oral communication skills; fluency in one or more additional European language(s) ideally French
  • IT skills: Microsoft Office, ideally knowledge of some statistics software.

 

In return, we offer an exciting and challenging position with great potential for personal development, with a unique organization in a fascinating and fast-growing medical industry. If you want to work in an enthusiastic, motivated team and help launch the hearing implants of the future then send us your online application in English. For further information please contact the clinical research department: clinicalresearch.intl@xxxxxxxxxxxxxxxxxxx. We favour disabled applicants over non-disabled applicants if they have the same qualification.

Sonova is an equal opportunity employer

We team up. We grow talent. We collaborate with people of diverse backgrounds to win with the best team in the market place. We guarantee every person equal treatment in regard to employment and opportunity for employment, regardless of a candidate’s ethnic or national origin, religion, sexual orientation or marital status, gender, genetic identity, age, disability or any other legally protected status.

 

 

 

 



Laure Arnold

SENIOR MANAGER CLINICAL RESEARCH INTERNATIONAL

twitter.com/AdvancedBionics

blog.advancedbionics.com

 

 

5, Rue Maryse Bastié CS 90606
69675 Bron Cedex, France
+33 4 72 14 54 60
www.AdvancedBionics.com 

 


Legal Notice:
The information in this electronic transmission may contain confidential or legally privileged information and is intended solely for the individual(s) named above. If you are not an intended recipient or an authorized agent, you are hereby notified that reading, distributing, or otherwise disseminating, copying or taking any action based on the contents of this transmission is strictly prohibited. Any unauthorized interception of this transmission is illegal under law. If you have received this transmission in error, please notify the sender by telephone [at the number indicated above/on +41 58 928 0101] as soon as possible and then destroy all copies of this transmission.
 

MID 04951