Senior Study Start-Up and Regulatory Lead

Ergomed seeks a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate activities to achieve site initiation readiness. You will provide regulatory expertise, ensure compliance, and act as a key liaison between internal teams, clients and external stakeholders. The role involves drafting, reviewing, and translating essential...

Ergomed seeks a Senior Specialist, Study Start Up and Regulatory Affairs to lead and coordinate activities to achieve site initiation readiness. You will provide regulatory expertise, ensure compliance, and act as a key liaison between internal teams, clients and external stakeholders. The role involves drafting, reviewing, and translating essential...

Every clinical trial begins with a critical first step – getting sites ready to enroll patients. In this role, you'll be the driving force behind regulatory and ethics submissions that open the door for breakthrough therapies to reach the people who need them. Your new role As a Senior Study Start-up Specialist, you will play a pivotal role in enabling...

Company DescriptionScorra verso il basso per una panoramica completa dei requisiti di questo lavoro. È la persona giusta per questa opportunità?Medicine moves forward here. So will you.Company DescriptionMedicine moves forward here. So will you.Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications....

Company Description Medicine moves forward here. So will you. Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability...

Company Description Medicine moves forward here. So will you. Company Description Medicine moves forward here. So will you. Ergomed is a specialist clinical research organization focused on rare disease and select oncology indications. We focus on the most complex trials, the studies where experience, judgement, and rigorous operational accountability...

Novo Nordisk Italy is seeking a Senior Study Start-up Specialist to enable clinical trials to launch on time and in compliance with local and international regulations. You will manage end-to-end study start-up, navigating regulatory landscapes to ensure sites are activated efficiently and patients access investigational treatments quickly.You will oversee...

For an innovative international biotechnology company, we are currently looking for an highly experienced Senior Director Regulatory Affairs (F/M/X) to lead the regulatory strategy and operations in Italy and support the preparation of a highly promising oncology launch. The Opportunity: The role provides strategic guidance across assigned projects,...

When our values align, there's no limit to what we can achieve.At Parexel, we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do.Each of us, no matter what we do at...