CTC Finance/ SrCPA

<p><span>Get ready to redefine what’s possible and discover your <b>extraordinary</b> <b>potential</b> at Labcorp. Here, you’ll have the opportunity to personally advance healthcare and make a difference in peoples’ lives with your bold ideas and unique point of view. With the support of <b>exceptional</b> <b>people</b> from across the globe and an <b>energized purpose</b>, you’ll be empowered to own your career journey with mentoring, training and personalized development planning.</span></p><p><span> </span></p><p><span>Join us as we speed the delivery of groundbreaking therapies and anticipate tomorrow’s drug development challenges, creating new possibilities for our clients—and your career.</span></p><p><span> </span></p><p><span>We have job openings for Clinical Trial Coordinators to be <b>office based in Paris, France. </b></span></p><p></p><p></p><p><b><span>The Clinical Trial Coordinator will support tasks associated with study start-up as well as experience with finance.</span></b></p><p></p><p><b><span>Responsibilities associated with this position:</span></b></p><p></p><p><b><span>1) Trial and site administration:</span></b><br /><span>o Tracking (e.g. essential documents) and reporting (e.g. Safety Reports)</span><br /><span>o Ensure collation and distribution of study tools and documents</span><br /><span>o Update clinical trial databases (CTMS) and trackers</span><br /><span>o Clinical supply & non‐clinical supply management, in collaboration with other country roles</span><br /><span>o Manage Labeling requirements and coordinate/sign translation change request</span><br /><span>• Document management:</span><br /><span>o Prepare documents and correspondence</span><br /><span>o Collate, distribute/ship, and archive clinical documents</span><br /><span>o Assist with eTMF reconciliation</span><br /><span>o Updating manuals/documents (e.g., patient diaries, instructions)</span><br /><span>o Document proper destruction of clinical supplies.</span><br /><span>o Prepare Investigator trial file binders</span><br /><span>o Execute eTMF Quality Control Plan</span><br /><span>o Obtain translations of documents</span></p><p><br /><b><span>2) Regulatory & Site Start‐Up responsibilities:</span></b><br /><span>o In a timely manner, provide to and collect from investigators forms/lists for site evaluation/validation, site start‐up and submissions</span><br /><span>o Obtain, track and update study insurance certificates</span><br /><span>o Support preparation of submission package for IRB/ERC and support regulatory agencies submissions.</span><br /><span>o Publish study results for GCTO and RA where required per local legislation</span></p><p><br /><b><span>3) Budgeting, Agreement and Payments: Collaborate with finance/budgeting representatives for:</span></b><br /><span>o Develop country and site budgets (including Split site budget)</span><br /><span>o Tracking, and reporting of negotiations</span><br /><span>o Maintenance of tracking tools</span><br /><span>o Working knowledge of Contract development, negotiation, approval and maintenance (e.g. CTRAs)</span><br /><span>o Update and maintain contract templates (in cooperation with Legal Department)</span><br /><span>o Payment calculation and execution (investigators, vendors, grants)</span><br /><span>o Ensure compliance with financial procedures</span><br /><span>o Monitor and track adherence and disclosures</span><br /><span>o Budget closeout.</span><br /><span>o Obtain and process FCPA documentation in a timely manner</span></p><p><br /><b><span>4) Meeting Planning:</span></b><br /><span>o Organize meetings (create & track study memos/letters/protocols)</span><br /><span>o Support local investigator meetings (invitations, prepare materials, select venue, support vendor where applicable</span></p><p></p><p><span><b>CTC Experiene requirements:</b></span></p><ul><li><span>Must be bilingual in French and English</span></li><li><span>Ability to drive and possess a valid driver’s license</span></li><li><span>Ability and willingness to present at internal and external meetings</span></li></ul><p></p><p><b>Labcorp is proud to be an Equal Opportunity Employer:</b></p><p></p><p>As an EOE/AA employer, the organization will not discriminate in its employment practices due to an applicant's race, age, color, religion, sex, national origin, sexual orientation, gender identity, disability or veteran status.</p><p></p><p>For <span>more information about how we collect and store your personal data, please see our </span><span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank">Privacy Statement</a></span><a href="https://www.labcorp.com/hipaa-privacy/web-privacy-policy" target="_blank"><span>.</span></a><span> </span></p>