Clinical Research Associate (m/f/d)

The Cardiac Management Solutions division of ZOLL Medical Corporation develops products to protect and manage cardiac patients, including the LifeVest® wearable cardioverter defibrillator (WCD), the ZOLL cardiac monitor, and associated technologies.

The LifeVest is a wearable defibrillator worn by patients at risk for sudden cardiac arrest (SCA), providing protection during their changing condition and while permanent SCA risk has not been established. The LifeVest allows a patient’s physician time to assess their long-term arrhythmic risk and make appropriate plans.

For our EMEA divison we are looking for a:

Clinical Research Associate (f/m/d) EMEA home based

(full time / unlimited)

Areas of Responsibility:

• Monitoring and site management activities for clinical research projects
• Acting as a company liaison, work with clinical sites to resolve any site related issues quickly and effectively
• Preparing of study related documents including but not limited to informed consent forms, note to file, etc.
• Monitor ongoing compliance to study protocols and site adherence to global regulatory guidelines, including safety reporting
• Responsible for the distribution, collection and tracking of regulatory documentation and support regulatory submissions
• Support clinical operations management in project management
• Partner with cross-functional teams (EMEA and US) such as data management and Medical affairs with query management, data reviews and resolution
• Coordinate or manage multiple projects across multiple centers and countries
• Travel to study sites based on project needs
• Performs other duties as assigned by Management
• Ability to travel up to 65%, based on project needs, including national and international conferences and responsibilities
• Participate in research meetings including presentations at those meetings

Experience and Personal qualities

• MS/PhD. in a clinical, scientific, or related field; and at least 3 years’ experience in medical industry
• Cardiology experience preferred
• Working knowledge of medical/scientific terminology and working knowledge of Ministry of Health regulations and GCP guidelines is required
• Knowledge of legal and regulatory landscape concerning clinical research
• Professional use of the English and German language, both written and oral
• Demonstrated proficiency in implementing, monitoring, and management of clinical trials (start-up to close-out)
• Presentation skills
• Facile in Microsoft Word, Office, Excel, and Project.

This is what we offer to you

• An attractive remuneration as well as an interesting and varied field of activity in a highly motivated, committed and harmonious team in the medical sector
• An attractive employer Contribution to company pension scheme

Have we sparked your interest? Then we look forward to receiving your application.

Do you have any question or You're not sure if your qualifications fit or you'd like to know more about the position first? Then give me a call!

Your contact person: Anja Preuße, HR Business Partner, Mobile: +49 (0) 151 549 54689; apreusse@zoll.com

You can find more information about us and our product at https://www.zoll.com/de and www.lifevest.zoll.com/de.