Specialist/Snr Specialist Study Start Up and Regulatory Affairs

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Medicine moves forward here. So willyou.
Ergomedis a specialist clinical research organization focused on rarediseaseand select oncology indications. We focus on the most complextrials,the studies where experience, judgement, and rigorous operational accountability make the biggest difference. We partner with small to midsize biotech companies to move promising therapies through early phase development, so they reach the patients sooner.
We choose complex work on purpose. Rare disease and oncology trials carry real operational risk, and our people are experts at reducing it, protecting timelines, dataqualityand the experience of sites and patients at the same time. It is demanding, meaningful work, and no one here forgets that patients cannot wait.
That is why culture matters to us as much as capability. We have built a collaborative, international team where people share ideas, growtheircareersand are trusted to take ownership early. With colleagues across North America, South America, Europe,Asiaand Australia, we value teamwork,flexibilityand a real commitment to work-life balance,



because good science comes from people who feel supported.
If you wantworkwith purpose, the agility to make an impact and a team that cares about the people behind the work as much as the work itself, we would love to hear from you.
The Senior Specialist, Study Start Up and Regulatory Affairs leads and coordinates all activities related
to achieving site initiation readiness. The role provides subject matter expertise, ensures regulatory
compliance, and serves as a key liaison between internal teams, clients, and external stakeholders
Accountable for delivery of assigned study start-up and regulatory milestones within definedscope.
Make independent decisions within assigned scope regarding regulatory processes anddocumentation approaches.
Handles medium-complexity regulatory environments, including multi-country requirementswhere applicable.
Leads study start-up and regulatory activitie

Vedi l’offerta su Go Lavoro: golavoro.it/annuncio-lavoro/8cykrs