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CRA- Clinical Research Administrator ([com.successfactors.picklist.b, OR, US) @ BIOTRONIK Corporate Services SE

[com.successfactors.picklist.b, OR, USOnsiteFull-time
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<table align="left" border="0" cellpadding="1" cellspacing="1"> <tbody> <tr> <td colspan="2"> <p><img alt="ProfTangQuiCRMger.jpg" src="https://biotronik.plateau.com/icontent/CUSTOM_eu/biotronik/self-managed/GLOBAL/RECRUITING/TAMPLATES/ProfTangQuiCRMger.jpg" style="width:890.0px;height:342.0px"></p> </td> </tr> <tr> <td colspan="2"> <p><span style=""><span> </span></span><br> <span style=""><span> <span>As one of the world’s leading manufacturers of cardio- and endovascular medical devices, BIOTRONIK<br> is headquartered in Berlin, Germany, and represented in over 100 countries by its global workforce of<br> more than 5,600 employees. The work of our committed, highly specialized, exceptionally skilled employees<br> results in crucial advancements in the world of cardiology and changes the lives of patients every day.</span></span></span></p> <p> </p> </td> </tr> <tr> <td colspan="2"><span><span style=""> Please join us as</span></span><br> <span> </span></td> </tr> <tr> <td colspan="2"> <img alt="" src="https://biotronik.plateau.com/icontent/CUSTOM_eu/biotronik/self-managed/GLOBAL/RECRUITING/TAMPLATES/Linie_Blue_Purple_890.jpg"></td> </tr> <tr> <td colspan="2"> <span> <span style=""><span contenteditable="false" tabindex="-1"><span><span>Interface Specialist to SAP</span></span></span> </span></span></td> </tr> <tr> <td colspan="2"> <p><span style=""><span> <span> </span></span></span><br> <span><span style=""> <span>Our department Health Services is responsible for Orerionsed qui tetur sit quae simint aborupt atectem qui aut<br> aute preperit, sunt evelibus alicae prepe vellesciur aut parum est lit, comnisc illaborerum harum eossimusam<br> voluptae officideria poremodit, oditates explia ipidel ea am volupta</span></span><br> </span></p> </td> </tr> <tr> <td><span style=""><span style=""><span> <span> Your Responsibilities</span></span></span></span><br> <span> </span> <ul style="list-style-type:square"> <li><span><span style="">Conception and Specification of</span></span></li> <li><span><span style="">Definition of product strategies</span></span></li> <li><span><span style="">Specification of new products</span></span></li> <li><span><span style="">Assistance in the market entry</span></span></li> <li><span><span style="">Assistance in the market entry</span></span></li> </ul> </td> <td><span><span style=""><span style=""> <span>Your Profile</span></span></span><br> <span> </span></span> <ul style="list-style-type:square"> <li><span><span style="">Conception and Specification of</span></span></li> <li><span><span style="">Definition of product strategies</span></span></li> <li><span><span style="">Specification of new products</span></span></li> <li><span><span style="">Assistance in the market entry</span></span></li> <li><span><span style="">Assistance in the market entry</span></span></li> </ul> </td> </tr> </tbody> </table> <p> </p> <table align="center" border="0" cellpadding="1" cellspacing="0" width="100%"> <tbody> <tr> <td> <div><strong>Ihre Aufgaben</strong><br> <br> Bei den Themen internationale Zulassung von hochkomplexen Medizinprodukten sowie nationale und internationale (prä- )klinischer Studien ist unsere Abteilung Regulatory &amp; Clinical Affairs in Ihrem Element.</div> <div><span style="text-decoration:none"><font color="white"><span style="text-decoration:none"><font color="white"><span style="text-decoration:none"><font color="white"><span style="text-decoration:none"><font color="white"> </font></span></font></span></font></span></font></span></div> <div> <ul> <li>Planen, Genehmigen, Durchführen und Überwachen von internationalen klinischen Studien unter Beachtung der behördlichen Auflagen und normativen Anforderungen</li> <li>Entwerfen, Abstimmen und Verabschieden von Studienprotokollen sowie Koordination der Studienteams</li> <li>Unterstützung und Überwachung der Budget- und Ressourcenplanung</li> </ul> </div> <br> </td> </tr> <tr> <td> <div><strong>Ihr Profil</strong></div> <div> </div> <ul> <li>Abgeschlossenes Studium in Medizin, Natur- oder Ingenieurwissenschaften</li> <li>Erste Erfahrungen in der Durchführung von klinischen Studien sowie Vorkenntnisse zu relevanten Vorschriften und Gesetzen (ISO 14155, GCP, MPG) wünschenswert</li> <li>Von Vorteil: Kenntnisse der Kardiologie und Elektrophysiologie</li> <li>Sehr gute Deutsch- und Englischkenntnisse</li> </ul> </td> </tr> </tbody> </table> <p> </p> <p> </p> <p> </p> <p> </p> <table border="0" cellpadding="1" cellspacing="1" style="width:890.0px"> <tbody> <tr> <td><br> <br> </td> <td> <p><br> <span style=""><strong> </strong></span><strong><a href="http://www.biotronik.com/karriere" target="_blank"><span style=""><span style="">www.biotronik.com/karriere</span></span></a></strong></p> </td> </tr> <tr> <td> <p><span style=""><span>Location: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span>2181</span></span></span></span> </span></span></p> <p><span style=""><span>Working hours: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span>Full-time</span></span></span></span> </span></span></p> <p><span style=""><span>Type of contract: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span>4823</span></span></span></span> </span></span></p> </td> <td> <p><span style=""><span>Job ID: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span>3641</span></span></span></span> </span></span></p> <p><span style=""><span>Contact: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span>[email protected]</span></span></span></span> </span></span></p> <p><span style=""><span>Tel.: <span contenteditable="false" tabindex="-1"><span contenteditable="false" tabindex="-1"><span><span></span></span></span></span></span></span></p> </td> </tr> <tr> <td colspan="2"> <p><span style=""><span>We are an equal opportunity employer and all qualified applicants will receive consideration for employment<br> without regard to race, color, religion, age, sex, sexual orientation, gender identity or expression, national origin,<br> disability status, protected veteran status, genetic information, or any other characteristic protected by law.</span></span></p> </td> </tr> </tbody> </table> <p> </p>

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