Clinical Trial Start-Up Specialist: 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...

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...

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 is seeking a Regulatory and Start Up Specialist based in Madrid to drive country/site activation for clinical trials. You will prepare submissions, interact with authorities and ethics committees, and coordinate with regulatory, clinical operations, and contracts teams to ensure timely approvals.You should have a life sciences degree...

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,...

Fortrea is seeking a Site Start-Up Specialist to coordinate site activation, manage essential documents, and ensure timely regulatory submissions. You will work with the FSPx team and regulatory authorities to accelerate clinical trials. The ideal candidate will have a life sciences background, 2+ years in clinical research, and strong organizational and...

Precision for Medicine is seeking a Regulatory and Start Up Specialist based in Madrid to drive country/site activation for clinical trials. You will prepare submissions, interact with authorities and ethics committees, and coordinate with regulatory, clinical operations, and contracts teams to ensure timely approvals. You should have a life sciences degree...

Regulatory and Start Up Specialist (Portuguese speaker) – Full time on site position in Madrid, MD, ES. 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...

Precision Medicine Group in Madrid, Spain, is seeking a Regulatory and Start Up Specialist for an on-site role. You will drive site activation, prepare CTAs and submission dossiers, and liaise with authorities and ethics committees to obtain approvals in line with ICH-GCP and local requirements.The ideal candidate will have CRO/pharma experience, strong...