Clinical Trial Start-Up Lead: Regulatory

Fortrea in Madrid seeks an experienced Site Regulatory & Contract Manager to lead country-level study start-up activities, ensuring trials are initiated on time, within budget, and in compliance with regulations and quality standards. The role requires at least 5 years of regulatory and start-up experience, strong project and stakeholder management, and...

BeOne seeks a Startup Specialist to manage and coordinate all activities related to the start-up of clinical trials at multiple sites. The role ensures timely initiation, regulatory compliance, and quality standards are met across countries.You will translate documents, oversee essential study materials, and work with investigators to retrieve critical...

Senior Project Manager At ICON Strategic Solutions, you will work in a sponsor-dedicated model, supported by ICON’s global expertise. As the world’s largest FSP organisation, with over 90 sponsor partnerships, we offer stability, career development and a collaborative environment where your work contributes to the development of treatments that benefit...

Ergomed Group is a specialist clinical research organization focused on rare disease and select oncology indications, with global presence and a collaborative culture. The Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related to achieving site initiation readiness and regulatory compliance.Role requires a graduate...

Roche recherche un Responsable Country Start-Up pour diriger la stratégie pays et optimiser les démarrages d’études cliniques, en assurant des soumissions réglementaires et une collaboration efficace avec les équipes transfrontalières.Le candidat idéal possède une expertise en démarrage d’essais, maîtrise de l’ICH-GCP et anglais et espagnol...

Precision for Medicine is seeking a Regulatory and Start Up Specialist based in Madrid to drive country/site activation for clinical trials.¿Es este el puesto que está buscando? Si es así, siga leyendo para obtener más detalles y no olvide enviar su solicitud hoy mismo.You will prepare submissions, interact with authorities and ethics committees, and...

Precision for Medicine is seeking a Regulatory and Start Up Specialist based in Spain to drive site activation readiness and manage regulatory submissions with authorities and ethics committees.Haga clic en "Solicitar" a continuación para enviar su candidatura. Asegúrese de que su CV está actualizado y de que ha leído primero las especificaciones del...

Responsible for delivering site activation readiness, managing regulatory submissions, contracts, and budget negotiations for clinical trials in Spain, requiring fluency in Portuguese and English.

Precision Medicine Group in Madrid, Spain, is seeking a Regulatory and Start Up Specialist for an on-site role.La siguiente información ofrece un resumen de las habilidades, cualidades y cualificaciones necesarias para este puesto.You will drive site activation, prepare CTAs and submission dossiers, and liaise with authorities and ethics committees to...