Emplois actuels liés à Clinical Trials Coordinator - Paris, Île-de-France - Excelya
-
Clinical Trial Coordinator
il y a 3 semaines
Paris, Île-de-France PSI Temps pleinJob Title: Site CoordinatorThe Site Coordinator role at PSI is a key position that supports a Clinical Study Site in clinical trial-related activities according to ICH-GCP and protocol requirements. This role is responsible for ensuring timely responses to feasibility questions, scheduling and preparation for monitoring visits, and tracking patient...
-
Clinical Trials Coordinator
il y a 2 semaines
Paris, Île-de-France IQVIA Temps pleinThe Research and Development Solutions team at IQVIA is dedicated to helping healthcare customers find innovative treatment solutions for various illnesses. As a Clinical Trials Assistant, you will provide administrative support to clinical teams, contributing to the research process. We seek dynamic and motivated individuals who want to make a difference in...
-
Clinical Trials Coordinator
il y a 3 semaines
Paris, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is dedicated to helping our healthcare customers find innovative treatment solutions for patients with various illnesses. As a Clinical Trials Assistant, you will provide administrative support to our clinical teams, contributing to the research and development of new treatments.The Clinical Trials Assistant...
-
Clinical Trials Coordinator
il y a 3 semaines
Paris, Île-de-France IQVIA Temps pleinAt IQVIA, we're seeking a highly organized and detail-oriented Clinical Trials Assistant to join our Research and Development Solutions team. This role will provide administrative support to our clinical teams, ensuring the smooth execution of clinical trials.Key Responsibilities:Assist Clinical Research Associates (CRAs) and Regulatory and Start-Up (RSU)...
-
Clinical Trials Coordinator
il y a 2 semaines
Paris, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is dedicated to helping healthcare customers find innovative treatment solutions for patients with various illnesses. As a Clinical Trials Assistant, you will provide administrative support to clinical teams, contributing to the research process.The Clinical Trials Assistant will be responsible for:Assisting...
-
Clinical Trials Coordinator
il y a 3 semaines
Paris, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team is dedicated to helping our healthcare customers find innovative treatment solutions for patients with various illnesses. As a Clinical Trials Assistant, you will provide administrative support to the clinical teams, contributing to the research and development of new treatments.The Clinical Trials Assistant...
-
Clinical Trial Coordinator
il y a 3 semaines
Paris, Île-de-France Pharmiweb Temps pleinClinical Trial Assistant RoleAt Pharmiweb, we're seeking a highly organized and detail-oriented Clinical Trial Assistant to join our team. As a Clinical Trial Assistant, you will play a crucial role in the coordination and administration of study activities from start-up to execution and close-out. Key responsibilities include:Creating and managing the Trial...
-
Clinical Trials Coordinator
il y a 3 semaines
Paris, Île-de-France IQVIA Temps pleinJoin Our Team as a Clinical Research Administrative AssistantIQVIA is a leading global provider of advanced analytics, technology solutions, and clinical research services to the life sciences industry. We are seeking a highly motivated and organized Clinical Research Administrative Assistant to join our team in France.About the RoleThe Clinical Research...
-
Clinical Trial Agreement Specialist
il y a 2 semaines
Paris, Île-de-France Pharmiweb Temps pleinClinical Trial Agreement SpecialistPharmiweb is seeking a highly skilled Clinical Trial Agreement Specialist to join our team. As a key member of our Clinical Contracting team, you will be responsible for preparing, negotiating, and finalizing clinical trial agreements and budgets related to clinical trials.Key Responsibilities:Prepare, negotiate, and...
-
Clinical Trial Agreement Specialist
il y a 4 semaines
Paris, Île-de-France ENGINEERINGUK Temps pleinJob SummaryWe are seeking a highly skilled Clinical Trial Agreement Specialist to join our team at ENGINEERINGUK. The successful candidate will be responsible for preparing, negotiating, and finalizing clinical trial agreements and budgets related to clinical trials. This is a challenging and rewarding role that requires strong communication and negotiation...
-
Clinical Trial Agreement Specialist
il y a 4 semaines
Paris, Île-de-France ICON Temps pleinJob Title: Clinical Trial Agreement SpecialistAt ICON, we are seeking a highly skilled Clinical Trial Agreement Specialist to join our team. As a key member of our Clinical Contracting team, you will play a critical role in the negotiation and management of clinical trial agreements with sites and investigators.Key Responsibilities:Negotiate and finalize...
-
Clinical Trial Agreement Specialist
il y a 3 semaines
Paris, Île-de-France ICON Temps pleinJob Title: Clinical Trial Agreement SpecialistAt ICON, we are seeking a highly skilled Clinical Trial Agreement Specialist to join our team. As a key member of our Clinical Contracting and Commercialization (CCS) team, you will play a critical role in negotiating and finalizing clinical trial agreements and budgets.Key Responsibilities:Negotiate and finalize...
-
Clinical Trial Site Manager
il y a 3 semaines
Paris, Île-de-France Clariness Temps pleinClinical Trial Site Management OpportunityWe are seeking a skilled Medical Customer Service Representative to manage clinical trial sites and ensure patient recruitment. The ideal candidate will have a strong understanding of medical topics and experience in handling customer requests via phone and email. Key Responsibilities:Screen patients for clinical...
-
Clinical Trial Contract Specialist
il y a 3 semaines
Paris, Île-de-France Pharmiweb Temps pleinJob SummaryWe are seeking a skilled Clinical Trial Contract Specialist to join our team at Pharmiweb. As a key member of our Clinical Contracting team, you will play a critical role in preparing, negotiating, and finalizing agreements and budgets related to clinical trials.Key ResponsibilitiesAgreement Preparation and Negotiation: Prepare, negotiate, and...
-
Quality Assurance Specialist
il y a 3 semaines
Paris, Île-de-France Snitem Temps pleinJob DescriptionCarthera is a French clinical-stage medtech company developing innovative ultrasound-based medical devices. We are seeking a Quality Assurance Specialist - Clinical Trials to join our team in Lyon, France. The successful candidate will be responsible for ensuring the quality of clinical trials and ensuring compliance with regulatory...
-
Clinical Trials Project Manager
il y a 3 semaines
Paris, Île-de-France Cromos™ Pharma Temps pleinJob Title: Clinical Trials Project ManagerCromos Pharma is seeking a highly skilled Clinical Trials Project Manager to join our team. As a key member of our project management team, you will be responsible for coordinating and managing clinical trials from start to finish.Key Responsibilities:Establish and maintain relationships with customers and...
-
Quality Assurance Manager
il y a 3 semaines
Paris, Île-de-France Snitem Temps pleinCarthera, a French clinical-stage medtech company, is seeking a Quality Assurance Manager to join its clinical team in Lyon, France. The successful candidate will be responsible for ensuring the quality of clinical trials, adhering to good clinical practices and regulatory requirements. The Quality Assurance Manager will work closely with the clinical team...
-
Clinical Trials Assistant
il y a 2 jours
Paris, Île-de-France IQVIA Temps pleinThe IQVIA Research and Development Solutions team drives innovation in the life sciences industry by helping our healthcare customers find effective treatments for patients. As a Clinical Research Administrative Assistant, you will provide administrative support to our clinical teams, contributing to the research and development of new treatments.Key...
-
Senior Clinical Research Associate – Global Clinical Trials
il y a 2 semaines
Paris, Île-de-France Allucent Temps pleinAbout the RoleWe are seeking a highly experienced Senior Clinical Research Associate to join our global clinical trials team at Allucent. As a key member of our team, you will be responsible for monitoring and managing clinical studies to ensure compliance with regulatory requirements and Good Clinical Practice.Key ResponsibilitiesIndependently monitor and...
-
Clinical Trials Project Manager
il y a 4 semaines
Paris, Île-de-France Cromos™ Pharma Temps pleinJob Title: Clinical Trials Project ManagerCromos Pharma is seeking a highly skilled Clinical Trials Project Manager to join our team. As a Clinical Trials Project Manager, you will be responsible for coordinating local project activities, establishing new customer relationships, and maintaining existing customer relationships.Key Responsibilities:Coordinate...
Clinical Trials Coordinator
Il y a 2 mois
Excelya, a people-centered Contract Research Organization (CRO), is seeking a highly skilled Clinical Trials Assistant to join our team. As a Clinical Trials Assistant, you will play a crucial role in supporting the clinical project management and monitoring of clinical studies.
Key Responsibilities:- Support the clinical project management and monitoring of clinical studies, including liaison with monitors, CROs, drug vendors, central laboratories, and other vendors.
- Be an active member of the study team and take responsibilities for service provider oversight for his/her scope of responsibility according to procedures.
- Monitor, verify, and archive the Trial Master File as per SOPs, instructions, and trainings.
- Follow up and review of financial documents, in collaboration with GCPM.
- Create and update financial information within financial systems (SAP, K2) as need be as per study progress and service provider contract modification.
- Help to prepare forecast and assist at quarterly review meetings of study budget with GCPM and local finance controlling department.
- At least 3 years of work experience and training in clinical operations in a similar role.
- Substantial administrative experience or qualified to degree level.
- Fluent in English/Strong intermediate level proficiency.
- Basic Financial Knowledge.
- Knowledge of regulatory documents or medical terminology is recommended.
- Experience of working with multidisciplinary groups and ability to work within a team environment.
- Experience of managing and developing relationships with international Service Providers (SPs).
- Experience of tracking and manipulating clinical study documents and provider invoices.
- Strong organizational and communication skills.
Excelya offers a stimulating professional environment that encourages personal, intellectual, and operational participation. We commit to giving each Excelyate the means to express their natural talents, develop their full potential, and invest their unique selves in our unique project.
