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Clinical Trial Assistant ( CTA ) – sponsor-dedicated

Laboratory Corporation of America Holdings (Covance)

Lucerne, Luzern, Switzerland

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><span style="font-family: 'times new roman', times; font-size: 12pt;"><strong>Clinical Trial Assistant ( CTA ) – sponsor-dedicated</strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Location: Lucerne, Switzerland</span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">As a CTA at Labcorp, you are central to the successful delivery of complex clinical trials (phases I-III) in Switzerland. Not only will this position allow you to be close to the latest scientific breakthroughs across a wide variety of therapeutic areas, while collaborating with the most important pharmaceutical companies and the most innovative biotech organizations in the world - your work has a genuine impact on improving the health and lives of thousands of patients every day.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">If you are looking for a rewarding position in which you can leverage your organizational as well as your people skills, whilst gaining exposure within a world-class pharmaceutical working environment, this is an excellent opportunity. Join us and experience why more than 90% of the top 20 global pharmaceutical companies are repeat customers!</span></p><p style="margin-bottom: .0001pt;"> </p><p style="margin-bottom: .0001pt;"><span style="font-family: calibri, sans-serif;"><strong><span style="font-size: 10.0pt;">What you can expect from us:</span></strong></span></p><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Rewarding work in a stable, diverse, respected and highly profitable company</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">A thorough onboarding with support from your personal mentor</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Flexible working hours and compensatory time off in lieu</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">A permanent employment contract with Labcorp Drug Development</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Travel time = work time</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Highly competitive compensation packages</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Regular, merit-based salary adjustments</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Significant employer contribution to an attractive pension scheme</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Employer-financed life, accidental death and disability insurances</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Excellent training and career development opportunities as well as support with advancing your education</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">A genuine work life balance</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Strong support from Line Management and more than 20'000 colleagues worldwide</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">The world's most renowned pharmaceutical companies as our satisfied, repeat customers for many years</span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-family: calibri, sans-serif;"><strong><span style="font-size: 10.0pt;">Your responsibilities:</span></strong></span></p><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support project teams in all administrative aspects around clinical trials: trial and site administration, document management, regulatory and site start-up responsibilities, budgeting / contracts / payments, meeting planning</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 accurate, audit-ready data in clinical investigator files and databases</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></ul><h2>Education/Qualifications:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Degree in a relevant field such as life sciences, (veterinary) medicine, pharmacology, biology, chemistry, biochemistry, health care, health management, nursing etc.</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">In lieu of the above, a completed vocational education or professional experience (e.g. as study nurse, study coordinator) in a relevant field</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Professional experience in clinical research / drug development</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Basic understanding of biology and biological processes </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Familiarity with and/or practical application of ICH guidelines and GCP / GDP</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Proficient user of IT applications such as MS Office and clinical software - e.g. study databases, eTMF ( Veeva Vault etc.)</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-size: 10pt; font-family: calibri, sans-serif;">Excellent communication skills in business fluent German and English – verbal and written – and strong interpersonal skills are a must</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">French language skills a definite plus</span></li></ul><p style="margin-left: 36.0pt;"><span style="font-size: 12pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">#LI-AR1</span></p>

Job posted: 2021-11-24

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