Clinical Trial Start-Up Lead: Regulatory

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...

Manages and coordinates clinical trial start-up activities across multiple sites, ensuring timely initiation, regulatory compliance, and quality standards. Involves document translation, oversight of study materials, and retrieval of critical documents.

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. 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 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 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,...

Ergomed is seeking a Regulatory Start-Up Specialist to lead and coordinate all regulatory activities ensuring site initiation readiness for multi-country trials. You will ensure compliance with ICH-GCP and country-specific requirements, manage essential documents, and support risk management and strategic input across internal and external stakeholders. You...

Fortrea Spain S.A. seeks a Site Regulatory & Contract Manager to lead country-level study start-up and regulatory submissions, ensuring trials activate on time and within budget. You will coordinate with Clinical Trial Coordinators, CRAs, regulatory, legal, finance and vendors, manage CTRAs and oversee quality, risk, and timelines across multiple studies in...