Trainee / Internship Clinical Trial Coordinator (6 months)

<h2>Job Overview:</h2><p style="margin-bottom: 3.0pt;"><strong><span style="font-size: 12.0pt; font-family: 'Times New Roman',serif;">Trainee / Internship Clinical Trial Coordinator (6 months)</span></strong></p><p style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Location: Paris, France</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;"><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-bottom: 3.0pt;"><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;">In this role, you will work closely with our sponsor-dedicated clinical trials teams, gaining insight into all stages of drug development processes and helping us advance the development of innovative, life-changing medications for therapies across a wide spectrum of indications: oncology, vaccines, cardiovascular, neurology, etc. <strong>This internship is explicitly designed to enable you for a permanent position at Labcorp Drug Development if you so wish</strong> - so if you are looking for a chance to learn all about what it takes to safely bring new, life-improving drugs to market, this is an excellent opportunity! </span></p><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: 'times new roman', times;"><strong><span style="font-size: 10.0pt; color: #2d2d2d;">Your responsibilities: </span></strong></span></p><ul><li style="color: #2d2d2d;"><span style="font-size: 10pt; color: #333333; font-family: calibri, sans-serif;">Support in ensuring that the research site investigator(s) and study personnel are conducting studies according to clinical protocols, SOPs, GCP and other applicable regulatory requirements</span></li><li style="color: #2d2d2d;"><span style="font-size: 10pt; color: #333333; font-family: calibri, sans-serif;">Ensure identification and reporting of safety issues</span></li><li style="color: #2d2d2d;"><span style="font-size: 10pt; color: #333333; font-family: calibri, sans-serif;">Help coordinate meetings with internal and external stakeholders</span></li></ul><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support in distributing and tracking safety reports </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Help prepare, update, record, collate, distribute, archive and dispose of documents (electronical and physical files)</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Create and maintain trackers as appropriate and needed</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Ensure and maintain accurate, up to date data in various clinical databases and applications </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Help coordinate meetings, payments and trial logistics</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Support document archiving management </span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Assist with contract and budget management</span></li></ul><h2>Education/Qualifications:</h2><ul style="margin-top: 0cm;"><li style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">Studying for a degree in a relevant field such as life sciences, biology, health care (management), nursing, pharmacology, (veterinarian) medicine, oecotrophology etc. </span></li><li style="margin-bottom: 3.0pt;"><span style="font-size: 10pt; font-family: calibri, sans-serif;">In lieu of the above, working on a valid certification in health / life sciences by an accredited institute</span></li></ul><h2>Experience:</h2><ul><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">An academic  or professional background in life sciences</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">A healthy curiosity and an eagerness to learn</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Awareness of applicable clinical research regulatory requirements such as Good Clinical Practice (GCP) and International Conference on Harmonization (ICH)</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">IT literate, including Microsoft Word, Excel, PowerPoint and preferably eTMF solutions such as Veeva Vault</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Effective time management and organizational skills, a professional demeanor and a keen attention to detail</span></li><li><span style="font-size: 10pt; font-family: calibri, sans-serif;">Ability to establish and maintain effective, trustful working relationships with internal and external stakeholders</span></li><li><span style="font-family: calibri, sans-serif;"><strong><span style="font-size: 10.0pt;">Excellent communication skills in both French and English –spoken and written - are a must</span></strong></span></li></ul><p style="margin-bottom: 3.0pt;"><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;">#LI-AR1</span></p>