Global Regulatory Affairs Lead – E-Invoicing

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...

Werfen, a growing diagnostics company founded in 1966 in Barcelona, Spain, provides regulatory support for its own and customer products. This role ensures documentation is prepared and submitted according to country legislation and that new regulatory requirements are implemented. Key accountabilities include obtaining CE and FDA registrations, maintaining...

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...

Job Overview Individual contributor with advanced knowledge acquired from at least 8 years of relevant industry experience. Working independently with limited supervision, the individual will provide strategic regulatory expertise and leadership for clinical trial applications and lifecycle management activities, with a strong focus on EU Clinical Trials...

Worldwide Clinical Trials is a global CRO seeking a senior Regulatory Affairs professional to lead regulatory submissions across EMEA, Asia Pacific, and Latin America, ensuring ongoing compliance with evolving regulations and key regulatory documents. You will coordinate ethics submissions, provide strategic regulatory guidance, and mentor junior staff while...

Worldwide Clinical Trials is a global CRO seeking a senior Regulatory Affairs professional to lead regulatory submissions across EMEA, Asia Pacific, and Latin America, ensuring ongoing compliance with evolving regulations and key regulatory documents.You will coordinate ethics submissions, provide strategic regulatory guidance, and mentor junior staff while...

Werfen, founded in 1966 and headquartered in Barcelona, Spain, is a world leader in diagnostics. This Regulatory Affairs position provides effective support for regulatory submissions and compliance for our products and customers.The role involves preparing CE and FDA documentation, liaising with Spanish authorities, maintaining files, and collaborating with...

Thomson Reuters is seeking a Senior Regulatory Associate to join the Regulatory Affairs team in Madrid. You will navigate global regulatory frameworks for e-invoicing and CTC, working with product, marketing, and external experts to ensure compliance and strategic alignment across jurisdictions. The role emphasizes collaboration, cross-functional education,...

Thomson Reuters is seeking a Senior Regulatory Associate to join the Regulatory Affairs team in Madrid. You will navigate global regulatory frameworks for e-invoicing and CTC, working with product, marketing, and external experts to ensure compliance and strategic alignment across jurisdictions.The role emphasizes collaboration, cross-functional education,...