CMS

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.

Our EMEA team is looking for a dedicated and motivated Clinical Research Associate (CRA) to support us in the execution and monitoring of clinical trials. In this role, you will play a key part in ensuring the quality and integrity of our clinical research projects from planning through to implementation.

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

(full time / unlimited)

Areas of Responsibility:

Monitoring and site management activities for clinical research projectsActing as a company liaison, work with clinical sites to resolve any site related issues quickly and effectivelyPreparing 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 reportingResponsible for the distribution, collection and tracking of regulatory documentation and support regulatory submissionsSupport clinical operations management in project managementPartner with cross-functional teams (EMEA and US) such as data management and medical affairs with query management, data reviews and resolutionCoordinate or manage multiple projects across multiple centers and countriesTravel to study sites based on project needsPerforms other duties as assigned by ManagementAbility to travel up to 65%, based on project needs, including national and international conferences and responsibilitiesParticipate in research meetings including presentations at those meetings

Experience and Personal qualities

MS/PhD. in a clinical, scientific, or related field; and ideally 3 years plus experience in medical industryCardiology experience preferredStrong working knowledge of medical/scientific terminology and working knowledge of Ministry of Health regulations and GCP guidelines is requiredKnowledge of legal and regulatory landscape concerning clinical researchProfessional use of the English language, both written and oral and one other Major European language (preferably French, Italian or Spanish)Demonstrated proficiency in implementing, monitoring, and management of clinical trials (start-up to close-out)Presentation skillsFacile in Microsoft Word, Office, Excel, and Project.

This is what we offer

A varied job with plenty of development potential in a dynamic and growing medical technology marketFlexible and convenient working hours and 30 days annual leaveTake advantage of our numerous training opportunities and grow with usBenefit from various discounts on our corporate benefit portalYour health is important to us: benefit from our varied health management programComprehensive training in your area of responsibility is a matter of course for us

If this opportunity is of interest to you, we look forward to receiving your application documents.

Question? If you are unsure whether your qualifications are suitable or would like further information about the position, please give me a call.

Your contact is Anja Preuße, Senior HR Business Partner.

You can reach me by phone on +49 (0) 2236 8787 589 or by email at apreusse@zoll.com.