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Clinical Project Assistant - sponsor-dedicated - office-based, Munich

Laboratory Corporation of America Holdings (Covance)

Munich, Germany

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><strong><span style="font-family: 'times new roman', times; font-size: 12pt;">Clinical Project Assistant - sponsor-dedicated - office-based, Munich</span></strong></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Location: Munich, Germany</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; color: windowtext; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-family: calibri, sans-serif; font-size: 10pt;"><span style="color: windowtext;">Labcorp Drug Development has supported the pharmaceutical industry worldwide in developing more medicines than any other company, including the top 50 best-selling drugs on the market today. Our</span><span style="color: windowtext;"> highly dedicated, supportive teams work on bringing drugs to market that have a real impact on the lives and health of people.</span></span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"> </p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-family: calibri, sans-serif; font-size: 10pt;"><span style="color: windowtext;">If you bring professional experience in a similar role supporting clinical trials (phase II-IV), are business fluent in German and English and are looking for a position in which you can leverage your organizational skills as much as your talent to connect and communicate with a wide variety of people, this is the perfect opportunity. </span><span style="color: windowtext;">Join us and see why more than 90% of the top 20 global pharmaceutical companies are repeat customers. </span></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><div><strong><span style="font-family: calibri, sans-serif; font-size: 10pt;">What we have to offer: </span></strong></div><ul><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">flexible working hours, capped overtime and compensatory time off in lieu</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">a permanent employment contract</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">travel time = work time</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">highly competitive compensation packages including Christmas and vacation allowances</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">regular, merit-based salary adjustments</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">significant employer contribution to an attractive pension scheme</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">excellent training and career development opportunites as well as support with furthering your education</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">strong support from Line Management and more than 20'000 colleagues worldwide</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;">the world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years</span></li></ul><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><strong><span style="font-family: calibri, sans-serif; font-size: 10pt;">Your responsibilities:</span></strong></p><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support project teams with administrative clinical trial activities from study / site start up and management to site closure, owning processes such as document management, regulatory submission deadlines, meeting organization, etc.</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Coordinate internal and external stakeholders, facilitating smooth processes and top quality</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Set up and maintain clinical investigator files and documentation</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Prepare investigator budget payments and tracking systems; generate tracking reports </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Enter and maintain data into selected study tracking databases and ensure a high level of data quality</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Prepare monitoring visit documentation for CRAs, Project Managers etc.</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Oversee appropriate archiving of study documents and other materials</span></li></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Degree or completed vocational training (office management, administration, health care, life science or similar preferred) or equivalent professional experience</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">First professional experience in a comparable role as Clinical Trial Administrator, Clinical Project Assistant, Cllnical Trials Coordinator, study nurse, research nurse, etc.</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Familiarity with clinical research / trial processes and their local as well as international regulations, including ICH/GCP</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Experience with study start-up scenarios, submissions to the German regulatory authorities, site management and / or contract management a plus</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Proficient user of IT applications such as MS Office (including MS Excel) and clinical trial solutions such as eTMF (e.g. Veeva Vault)</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Strong organizational and project management skills with a keen attention to detail and a high sense of accountability</span></li><li><span style="font-family: calibri, sans-serif; font-size: 10pt;"><strong>Excellent communication skills in business fluent German and English – verbal and written – and strong interpersonal skills are a must</strong></span></li></ul><p style="margin: 0px;"> </p><p style="margin: 0px;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">#LI-AR1</span></p>

Job posted: 2021-10-12

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