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Clinical Project Assistant – sponsor-dedicated - Paris

Laboratory Corporation of America Holdings (Covance)

Paris, France

<h2>Job Overview:</h2><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 12.0pt; font-family: 'Times New Roman',serif;">Clinical Project Assistant – sponsor-dedicated - Paris</span></strong></p><p style="margin-bottom: .0001pt;"><span style="font-family: calibri, sans-serif;"><strong><span style="font-size: 10.0pt;">Location: Paris, France</span></strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">A formula for clinical innovation: Labcorp Drug Development. With comprehensive drug development services and de-identified data from 70 million patients worldwide, our 60,000 employees advance life-changing medicines across a wide range of therapeutic areas – improving health and lives every day.</span></p><p style="margin: 0cm 1.7pt .0001pt 0cm;"><span style="font-family: calibri, sans-serif;"><span style="font-size: 10pt; color: windowtext;">If you are looking for a position in which you can leverage your organizational skills and your clinical expertise as much as your talent to connect and communicate with a wide variety of people, this is the perfect opportunity! </span><span style="font-size: 10pt; 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: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;"> </span></p><p style="margin-bottom: 3.0pt;"><strong><span style="font-size: 10.0pt; font-family: 'Times New Roman',serif;">What you can expect from us:</span></strong></p><ul style="margin-top: 0cm;"><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">flexible working hours, capped overtime and compensatory time off in lieu</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">permanent employment contract with Labcorp Drug Development</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">travel time = work time</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">highly competitive compensation packages</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">subsidized meals and transportation allowances</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">bonus schemes / profit sharing</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">regular, merit-based salary adjustments</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">significant employer contribution to an attractive pension scheme</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">extensive insurance coverage, including medical, life, short as well as permanent disability and accidents</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">excellent training and career development opportunites as well as support with furthering your education</span></li><li style="color: #333740; margin-bottom: 3.0pt;"><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 style="color: #333740; margin-bottom: 3.0pt;"><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;"> </p><p style="margin-bottom: .0001pt;"><strong><span style="font-size: 10.0pt; font-family: 'Times New Roman',serif;">Your responsibilities:</span></strong></p><ul style="margin-top: 0cm;"><li style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support project teams in the full spectrum of clinical research activities such as study start up, site management / closure, document management (eTMF and paper-based), regulatory and site start-up responsibilities, meeting planning</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Coordinate internal and external stakeholders, facilitating smooth processes and top quality</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Administrative support of various contract teams including approvals, quality assurance and document management (contract databases and / or paper-based)</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Set up and maintain clinical investigator files and documentation</span></li><li style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Prepare investigator budget payments and tracking systems; generate tracking reports</span></li><li style="margin-bottom: .0001pt;"><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 style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Prepare monitoring visit documentation for CRAs, Project Managers etc.</span></li><li style="margin-bottom: .0001pt;"><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 style="margin-bottom: .0001pt;"><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 experience in a comparable role including familiarity with submission / study start up processes</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Familiarity with French as well as international regulations around clinical trials (ICH, GCP etc.) and the French regulatory authorities</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Proficient user of IT applications such as MS Office (including strong MS Excel skills) and clinical IT applications (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;"><strong><span style="font-size: 10.0pt;">Excellent communication skills in business fluent French and English – verbal and written – and strong interpersonal skills are a must</span></strong></span></li></ul><p style="margin-bottom: .0001pt;"><span style="font-family: calibri, sans-serif;"><strong><span style="font-size: 10.0pt;"> </span></strong></span></p><p style="margin-bottom: .0001pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">#LI-AR1</span></p>

Job posted: 2021-10-08

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