Trabajo de Clinical Study Coordinator en Provincia de Ceuta

Descripción del trabajo In a nutshell Puede obtener más detalles sobre la naturaleza de esta vacante y lo que se espera de los solicitantes leyendo la información a continuación. Position: Clinical Study Coordinator Location: Madrid, Hibrid Experience 4+ years in international clinical trial coordination Want to know more? mAbxience is a global biopharmaceutical company committed to innovation...

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are...

A leading clinical research company in Spain is seeking a project manager for clinical studies. This role includes managing site selection, ensuring compliance with regulations, and training site staff. Candidates should hold a bachelor's degree in biomedical or medical science, have at least 2 years of CRA experience, and be proficient in English. The position offers the opportunity to...

Clinical Project Manager – Neuroscience Research Are you passionate about advancing clinical research in neurodegenerative disorders? We are looking for a Clinical Project Manager to lead the planning, coordination, and execution of innovative clinical studies, including interventional trials and large-scale observational cohorts. Desplácese hacia abajo para ver todos los requisitos del puesto...

Are you passionate about data integrity, clinical research, and driving excellence through innovation? Join our Biometry team at BCCC and help shape the future of data management in clinical studies. ¿Tiene lo que se necesita para triunfar? La siguiente información debe ser leída atentamente por todos los candidatos. About the Role As a Clinical Data Manager , you will play a key role in...

The Senior Clinical Project Manager reports to the Clinical Operations Manager and is responsible to manage the local and international projects in compliance with contractual requirements, timelines, standard operating procedures and relevant regulations and legislations. He/she leads the internal study team allocated on his/her projects ensuring that all deliverables meet agreed expectations...

Overview This position is responsible for project management and study site management from site selection to initiation until monitoring and close-out of assigned clinical studies in accordance with Tigermed Jyton or sponsor SOPs, International Conference on Harmonization Good Clinical Practice standard (GCP), ISO***** and other applicable regulations. The position is responsible for ensuring...

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are...

Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Inscríbase ahora, lea los detalles del trabajo desplazándose hacia abajo. Verifique que posee las habilidades necesarias antes de enviar una solicitud. We are looking for someone who can autonomously carry on the work...

Una empresa biofarmacéutica global está buscando un Coordinador de Estudios Clínicos con más de 4 años de experiencia y un sólido conocimiento en la coordinación de ensayos clínicos internacionales. El candidato ideal supervisará la ejecución de ensayos, gestionará CROs y garantizará el cumplimiento de las regulaciones pertinentes. Se espera que tenga habilidades excepcionales de comunicación y...

Overview Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. Responsibilities Contribute to the management and...

A clinical research organization is seeking a Clinical Research Associate III - Study Start-Up and Maintenance in Ceuta, Spain. This role involves acting as the primary liaison between clinical sites and the project team during the study lifecycle. Candidates should have a Bachelor's degree in Life Sciences or a related field, with at least 5 years of study start-up experience in the clinical...

Overview Due to our ongoing global expansion, we have a great opportunity for a Regulatory Submissions Specialist to join our growing regulatory team in Taiwan, on a fully remote basis. Las cualificaciones, habilidades y toda la experiencia relevante necesaria para este puesto se pueden encontrar en la descripción completa a continuación. The Regulatory Submissions Specialist contributes to the...

Kapadi is a full service CRO that focuses on complex oncology indications including immunotherapy and cellular therapies. We know that innovative research requires innovative operations and we've built that into our culture, systems and processes. We have an infrastructure to enhance access to patients and integrated technology to provide higher quality and faster access to results. We are...