Clinical Trial Assistant

Clinical Trial Assistant – H/F AIXIAL Group  recherche son prochain talent en tant que Clinical Trial Assistant – H/F. Dont vos missions seront les suivantes  (liste non exhaustive) : Contribuer au suivi financier des factures, grille de surcoût et les notes des études (sous Excel ou autre outils) Contrôler de manière mensuelle...

Clinical Trial Assistant – H/F AIXIAL Group  recherche son prochain talent en tant que Clinical Trial Assistant – H/F. Dont vos missions seront les suivantes  (liste non exhaustive) : Contribuer au suivi financier des factures, grille de surcoût et les notes des études (sous Excel ou autre outils) Contrôler de manière mensuelle...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

Job Summary: Medpace is the leading CRO for Biotech companies and is continuing to add Clinical Trial Managers of different experience levels to join our Clinical Trial Management Group in France, particularly in our Lyon office. Clinical Trial Managers with expertise in Neuroscience and CNS are welcome to continue to work in their area of expertise or to...

Job Summary: Responsibilities: - Communicate and collaborate on global study activities; working closely with the project coordinator and clinical trial manager - Ensure timely delivery of recurrent tasks consistently with a high degree of accuracy - Compile and maintain project-specific status reports within the clinical trial management system - Interact...

**Job summary**: As a **Clinical Research Associate **you will be expected to actively participate in and manage the recruitment of potential investigators and perform CA and EC submissions. You will be responsible for monitoring of clinical sites, maintenance of study files, conduct of pre-study and initiation visits, liaison with vendors and other duties....

**Company Description** Our client is a Global CRO currently supporting various Pharmaceutical & Biotech companies globally. They offer a full service solution encompassing clinical & non-clinical development, peri-approval & market access. They are currently seeking a Clinical Contract Specialist office based in Lyon. Job Overview - Prepare & negotiate...

Job description We are seeking a skilled and dedicated Clinical Data Manager to join our team at Amaris Consulting - CRO. As a Clinical Data Manager, you will be responsible for overseeing the data management activities for clinical trials and research projects. You will work closely with cross-functional teams to ensure...

Job description Amaris Consulting is a leading global pharmaceutical and clinical research organization dedicated to advancing healthcare through innovative research and development. Our team is composed of passionate professionals committed to improving patient outcomes and advancing medical science. Position Overview:...

Nous poursuivons aujourd’hui notre développement et la structuration de nos équipes en France et aux USA afin d’avancer le développement de nos programmes et renforcer notre portefeuille de produits. Pour soutenir l’ensemble de notre équipe clinique et rattachée à notre Directrice des opérations cliniques, nous ouvrons donc un poste...

Parexel is in the business of improving the world’s health. We do this by providing a suite of biopharmaceutical services that help clients across the globe transform scientific discoveries into new treatments. From clinical trials to regulatory, consulting, and market access, our therapeutic, technical, and functional ability is underpinned by a deep...

Job Summary: The Clinical Research Associate position at Medpace offers the unique opportunity to have an **exciting career** in the research of drug and medical device development while **making a difference** in the lives of those around them. For those with a **medical and/or health/life science background** who want to explore the research field, ...

**Job summary**: As a **Regulatory Specialist **you will be expected to actively participate in all start up activities and perform CA and EC submissions. You will be responsible for communication with Regulatory Authorities and Ethics Committees and function as an expert for Regulatory issues in France. Reporting to **Clinical Operations Manager**, you will...

Job Summary: Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Project Coordinator to join our team. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: - Review incoming medical imaging...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based in Lyon, Regulatory Submissions Manager to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and...

Created in 2014, Excelya is a people-centered Contract Research Organization (CRO) that excels with care. We offer a personal and authentic experience within a young, ambitious health company on the path to becoming the clinical research leader in Europe thanks to our 800 Excelyates. Our unique one-stop provider service model - leveraging full-service,...

Job Summary: Our clinical operations activities are growing rapidly, and Medpace currently has multiple full-time leadership openings within our Clinical Operations team. This is a position with tremendous visibility within the company that plays a critical role in the financial, operational, and customer service success of our clinical trials....

Job description We are seeking a talented and experienced SAS Programmer to join our team. As a SAS Programmer at Amaris Consulting - CRO, you will play a key role in supporting the statistical programming activities for clinical trials and research projects. You will collaborate with cross-functional teams to ensure the...

Job Summary: Our clinical operations activities are growing rapidly, and we are currently seeking a full-time, office-based Regulatory Submissions Coordinator to join our Clinical Operations team. This position plays a key role in the clinical trial management process at Medpace. If you want an exciting career where you use your previous expertise and can...

Job Summary: Our imaging services are growing rapidly, and we are currently seeking a full-time, office-based Project Assistant to join our team in Lyon. If you want an exciting career where you use your previous expertise and can develop and grow your career even further, then this is the opportunity for you. Responsibilities: - Documents drafting,...