Emplois actuels liés à Clinical Trial Manager - Paris, Île-de-France - IQVIA
-
Clinical Trial Manager
Il y a 10 minutes
Paris, Île-de-France ICON plc Temps pleinClinical Trial Manager - France - HybridICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentWe are constantly looking for motivated, reliable and...
-
Clinical Trials Assistant
il y a 2 semaines
Paris, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is focused on helping our healthcare customers to find innovative treatments solutions for patients with the common, large or rarest illnesses. Providing administrative support to the clinical teams members could make your contribution to the research. We seek dynamic and motivated people who truly want to...
-
Local Trial Manager
Il y a 9 minutes
Paris, Île-de-France IQVIA Temps pleinParis, France | Full time | Home-based | R1520016Job OverviewProject Leads are an integral part of clinical trial delivery, liaising with clinical teams to improve patients' lives by bringing new drugs to the market faster. The Project Lead is an essential member of the core project team responsible for project delivery of clinical studies to meet...
-
Clinical Research Associate
Il y a 11 minutes
Paris, Île-de-France R&D Partners Temps pleinDrive the future of clinical trials as a CRA supporting a global center of excellence in high‑quality, patient‑focused research.R&D Partners is seeking a Clinical Research Associate (CRA) to support the Global Clinical Operations (GCO) Center of Excellence. This role involves conducting clinical trial activities in alignment with GCO's mission of...
-
Clinical Project Manager
Il y a 10 minutes
Paris, Île-de-France Excelya Temps pleinAbout the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. We believe in creating bold solutions and fostering an inclusive environment where collaboration and individual growth go hand in hand.This role is an exciting opportunity to contribute to a dynamic, ambitious team in Clinical Operations. You will play a critical...
-
Senior Field Clinical Engineer-Electrophysiology
il y a 6 jours
Paris, Île-de-France Boston Scientific Temps pleinAdditional Locations:France-Auvergne-Rhône-Alpes; Belgium-Diegem; France-Bourgogne-Franche-Comté; France-Bretagne; France-Centre-Val de Loire; France-Grand Est; France-Hauts-de-France; France-Normandie; France-Nouvelle-Acquitaine; France-Occitanie; France-Pays de la Loire; France-Provence-Alpes-Côte d'Azur; France-Voisins le Bretonneux;...
-
Senior Field Clinical Engineer-Electrophysiology
il y a 6 jours
Paris, Île-de-France bostonscientific Temps pleinAdditional Locations: France-Auvergne-Rhône-Alpes; Belgium-Diegem; France-Bourgogne-Franche-Comté; France-Bretagne; France-Centre-Val de Loire; France-Grand Est; France-Hauts-de-France; France-Normandie; France-Nouvelle-Acquitaine; France-Occitanie; France-Pays de la Loire; France-Provence-Alpes-Côte d'Azur; France-Voisins le Bretonneux;...
-
Clinical Research Director
Il y a 12 minutes
Paris, Île-de-France Excelya Temps pleinAbout the JobJoin Excelya, where Audacity, Care, and Energy define who we are and how we work. As a Clinical Research Director, you will have the opportunity to lead and manage clinical development programs, driving innovation in clinical research while building and mentoring a high-performing team.This role is integral to the success of our clinical trials...
-
Principal Clinical Data Science Lead
Il y a 2 minutes
Paris, Île-de-France ICON plc Temps pleinPrincipal Clinical Data Science LeadICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical developmentPrincipal Clinical Data Science...
-
Clinical Research Associate II
Il y a 11 minutes
Paris, Île-de-France Allucent Temps pleinBring your monitoring expertise to the forefront of innovation.We are looking for a Clinical Research Associate (CRA II) or Senior Clinical Research Associate (Sr. CRA)to join our A-team. As a CRA II / Sr. CRA at Allucent, you will independently control and monitor investigational sites, pro-actively detect issues, provide solutions to ensure clinical...
Clinical Trial Manager
Il y a 31 minutes
The IQVIA sponsor-dedicated Clinical Functional Service Partnerships (Clinical FSP) department is supporting our client's project team in the execution of clinical trials. Joining the team provides the opportunity to manage wide span of phases of clinical research projects in various therapeutic areas and to cooperate closely with one of our key clients.
We currently offer the exciting opportunity to join the team as Clinical Trial Manager in full-time and work home-based in France. In this role you will be accountable for the operational management of the component of clinical trials. Furthermore, you will need to gain oversight to assure achievement of trial recruitment commitment, timelines, budget and quality standards (Trial Preparation, Conduct and Closeout).
MAIN RESPONSIBILITIES
• Deliver the trial according to the clinical trial protocol, within trial timelines, and in compliance with ICH-GCP and all other relevant external regulations.
• Lead and support local trial team and investigative sites in timely preparation of required trial documents, contracts, and necessary approvals.
• Check that all Regulatory Requirements are satisfied prior to trial/site initiation.
• Ensure appropriate trial-specific training of CRO internal and external partners in line with Trial Training Plan.
• In collaboration with Site Monitoring Lead and CRAs, ensure provision of appropriate trial oversight for the trials by monitoring compliance of trial sites and team to GCP, local regulations, BI SOPs, and adherence to trial protocol.
• In collaboration with Site Monitoring Lead and CRAs, ensure adequate trial supply distribution to sites and timely data entry and cleaning, and on time Data Base Lock.
• In collaboration with Trial Resource Specialist and with support from CRAs as appropriate, ensures collection of required documents, with timely, complete, and compliant archiving of all relevant documents for the eTMF and CTR Appendices.
• Develop and maintain relationships with investigational sites and support CRAs in site contacts.
• Report and provide Client updates, exchange critical information and share trial conduction information, within regulatory and compliance burdens.
• Ensures all tasks are carried out in accordance with respective applicable SOPs, Business Practices, and regulatory requirements. Ensures that all interactions and engagements are carried out with the highest ethical and professional standards.
• Leads local CRO trial team to ensure integrity of trial conduct, assurance of patient safety, and that local component of trial is planned, conducted, and reported in line with regulatory requirements. Requires orchestration of local CRO trial team, and integration with other functions as necessary throughout planning, conduct and closeout of trial.
• Works within a complex GCP and regulatory environment and on global clinical trials with multidisciplinary, international teams and with various internal and external stakeholders including suppliers and investigational sites.
REQUIRED KNOWLEDGE, SKILLS AND EXPERIENCE
• Master's or higher-level degree preferable in life science.
• Long term experience in clinical research, including at least 2 years of clinical trial management experience and monitoring experience in France.
• Proven experience in site relationship management.
• Exceptional knowledge of applicable clinical research regulatory requirements, i.e., Good Clinical Practice (GCP) and International Conference on Harmonization (ICH) guidelines.
• Excellent understanding of project financials and effective vendor management.
• Effective communication skills, fluent language skills in English and French.
• High ability to work on abstract complex topics and to strategic thinking, as well as solution orientation.
• High organizational and planning skills, time management and prioritization skills while working on multiple projects.
• Excellent leadership and collaboration skills, and the ability to establish and maintain effective working relationships with coworkers, managers and clients. Ability to influencing business partners in matrix structures.
• High degree of self-accountability and commitment and a strong growth mindset to drive change and contribute actively to future leading transformation.
• Very good computer skills including working knowledge of Microsoft Word, Excel and PowerPoint.
• Flexibility to occasional business travel for client meetings.
• Ability to make decisions, bringing clarity to disparate information to inform actions and drive results.
Please apply with your English CV.
IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at
IQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism.
