Spain Regulatory Start-Up Expert

Job Overview Perform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities. Essential Functions Under general supervision, serve as...

Job OverviewPerform tasks at a country level associated with Site Activation (SA) activities in accordance with applicable local and/or international regulations, standard operating procedures (SOPs), project requirements and contractual/budgetary guidelines. May also include maintenance activities.Essential FunctionsUnder general supervision, serve as...

DescriptionAt Allucent™, we are dedicated to helping small-medium biopharmaceutical companies efficiently navigate the complex world of clinical trials to bring life-changing therapies to patients in need across the globe.We are looking for a Start-Up Associate II (SUA II) to join our A-team (hybrid*) in Madrid, Spain! The SUA coordinates and performs...

Precision for Medicine is a global Clinical Research Organization with uniquely integrated offering which enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

Precision for Medicine in Spain is seeking a Regulatory and Start Up Specialist to lead site activation and regulatory submissions in the Spanish market.¿Tiene las cualificaciones y habilidades adecuadas para este trabajo? Descúbralo a continuación y pulse en "solicitar" para ser considerado.You will coordinate with CA/EC, manage budgets, and ensure...

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. The role requires coordination with cross-functional teams to align timelines, budgets, and documentation. The ideal candidate will have a life sciences degree,...

Precision for Medicineis a global Clinical Research Organization with uniquely integrated offering which enables the science of precision medicine by combining novel clinical trial designs, industry-leading operational and medical experts, advanced biomarker and data analytics solutions, and an unequivocal real passion for rare diseases and oncology, in...

Precision for Medicine in Spain is seeking a Regulatory and Start Up Specialist to lead site activation and regulatory submissions for clinical trials in the region. The role requires strong contracts and budgeting negotiation experience, and collaboration with CA/EC, IRB/EC timelines, and site contracts management.The ideal candidate will be fluent in...

Performs country-level site activation activities for clinical research studies, ensuring compliance with regulations and project timelines. Serves as a point of contact for investigative sites and project teams.