Clinical Trial Coordinator Paris, France

When our values align theres no limit to what we can achieve. At Parexel we all share the same goal - to improve the worlds health. From clinical trials to regulatory consulting and market access every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us no matter what we do at Parexel contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally we do it with empathy and were committed to making a difference. Parexel are currently seeking an experienced Clinical Trial Coordinator to join our FSP team in France. Hybrid office-based in Paris with the flexibility to go to the office as a minimum of three days per week and based on the business need. Open to candidates with experience as Clinical Trial Assistant, Study Coordinator, Clinical Trial Coordinator, Project Support Associate, ICCS, CRA or similar. Play a pivotal role in some of the most significant clinical studies taking place today Single sponsor dedicated to a legendary pharmaceutical R&D powerhouse. A top 10 company and the name behind an incredible array of medicines, therapies and vaccines. Collaborate and learn alongside some of the industrys most experienced people. Working as a Clinical Trials Coordinator at Parexel FSP provides an exciting platform for your skills as well as the potential to develop into a variety of career paths. We make a difference in millions of lives. Well do the same for your career Primary Responsibilities The Clinical Trial Coordinator (CTC) will support the Clinical Research Manager (CRM) and other team members through the life cycle of the study from study start-up to study closure. Trial and site administration and support. Collaborate with finance / budgeting representatives. Interact with internal and external stakeholders (study sites, vendors etc.) in support of clinical study objectives. Tracking and reporting negotiations. Ensuring compliance with financial procedures. Maintenance of tracking tools and systems. Collate, distribute and archive clinical documents. Assist with electronic Trial Master File reconciliation. Budgeting Agreement and Payments: Collaborate with finance / budgeting representatives. Meeting Planning Planning of meetings with study sites, investigators and internal stakeholders to ensure study timelines and deliverables are met. Education and Experience B.A. / B.S. (Life Sciences preferred) or equivalent healthcare experience. Minimum 1-2 years in Clinical Research in a similar role. Fluent in Local Languages and business proficient in English (verbal and written). Good understanding of Global Country / Regional Clinical Research guidelines. Effective time management, organizational and interpersonal skills, conflict management. Effective communication with external customers (e.g. sites and investigators). Able to work independently. Who are Parexel Parexel supports clinical studies across the full range of therapeutic areas and we have longstanding partnerships with a vast client base. We supported the trials of most of todays top 50 best-selling drugs but equally we enable more niche drug developments that are critical to the well-being of many patients. Youll be an influential member of the wider team. Not quite the role for you Join Our Talent Community and well reach out with job alerts when positions that match your career interests become available. Well also share periodic updates about the latest company news and events. Employment Type: Full‑Time Vacancy: 1 #J-18808-Ljbffr