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<p><span style=""><span>Unsere Abteilung...</span></span><span style=""><span> </span></span>(kopieren Sie den Inhalt dieses Fensters in das Feld Stellenbeschreibung.</p>
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<td style="width:445.0px;text-align:left"><span style=""><span style=""><span>Ihre Aufgaben</span></span></span><br>
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<td style="width:445.0px;text-align:left"><span style=""><span style=""><span>Ihr Profil</span></span></span><br>
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<li><span style=""><span>Bitte ersetzen</span></span></li>
<li><span style=""><span>Definition of product strategies</span></span></li>
<li><span style=""><span>Specification of new products</span></span></li>
<li><span style=""><span>Assistance in the market entry</span></span></li>
<li><span style=""><span>Assistance in the market entry</span></span></li>
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<li><span style=""><span>Bitte ersetzen</span></span></li>
<li><span style=""><span>Definition of product strategies</span></span></li>
<li><span style=""><span>Specification of new products</span></span></li>
<li><span style=""><span>Assistance in the market entry</span></span></li>
<li><span style=""><span>Assistance in the market entry</span></span></li>
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<p><span style=""><span>Haben wir Ihr Interesse geweckt? Dann bewerben Sie sich bitte online! Wir freuen uns auf Sie.</span></span></p>
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<p><span style=""><span>The Medical Affairs Group is responsible for the design, conduction and evaluation of international first-in-man, regulatory submission and post-marketing trials.</span></span></p>
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<td style="width:445.0px;text-align:left"><span style=""><span style=""><span>Your Responsibilities</span></span></span></td>
<td style="width:445.0px;text-align:left"><span style=""><span style=""><span>Your Profile</span></span></span>
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<li><span style="">Leading discussions and negotiations with notified bodies and authorities to discuss clinical strategy for the approval of our products</span></li>
<li><span style="">Take ownership and responsibility in providing scientific/ clinical input into the phases of product development steps as defined in procedure</span></li>
<li><span style="">Planning and writing of clinical evaluation reports taking into account current laws and regulations</span></li>
<li><span style="">Interact with different departments and functions including R&D, RA, Risk and Validation, clinical study managers, biostatisticians and clinical investigators</span></li>
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<li><span style="">PhD/MD in medicine, life or health sciences</span></li>
<li><span style="">At least 5 years experience in medical writing, with minimum of 3 years in medical device or pharma industry</span></li>
<li><span style="">Ability to interpret complex clinical data and good knowledge and understanding of statistics</span></li>
<li><span style="">Experience with conducting extensive medical literature searches and reviews using various database sources such as PubMed</span></li>
<li><span style="">Team oriented, confident and proactive personality with an analytical working style</span></li>
<li><span style="">Excellent command of spoken and written English and German</span></li>
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<p><span><span style="">Are you interested? Please apply online! We are looking forward to welcoming you.</span></span></p>
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<td colspan="2" style="width:890.0px"> <img alt="" src="https://biotronik.plateau.com/icontent/CUSTOM_eu/biotronik/self-managed/GLOBAL/RECRUITING/TAMPLATES/Linie_Blue_Purple_890.jpg" style="width:890.0px;height:20.0px"></td>
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<p><span style=""><span>Standort: <span>6901</span></span></span> <span style=""><span> </span></span></p>
<p><span style=""><span>Arbeitszeit: Vollzeit </span></span></p>
<p><span style=""><span>Vertragsart: <span>befristet</span></span></span> <span style=""><span> </span></span></p>
<p><span style=""><span>Erreichbare Entgeltgruppe: EG09</span> </span></p>
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<p><span style=""><span>Kennziffer: 6261 </span></span></p>
<p><span style=""><span>Abteilung:</span></span></p>
<p><span style=""><span>Ansprechpartner HR: <span>Recruiting Specialist TU</span></span></span> <span style=""><span> </span></span></p>
<p><span style=""><span>Tel.: </span></span></p>
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<p><span style=""><span>Schwerbehinderte Menschen werden bei gleicher Eignung bevorzugt berücksichtigt. Es besteht grundsätzlich auch die Möglichkeit der Teilzeitbeschäftigung. </span></span></p>
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