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 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, data quality and 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, grow their careers and are trusted to take ownership early. With colleagues across North America, South America, Europe, Asia and Australia, we value teamwork, flexibility and a real commitment to work-life balance, because good science comes from people who feel supported.
If you want work with 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 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
When you join Ergomed Group, you make a difference by helping to bring safe and effective pharmaceutical treatment to patients around the world. You’ll join a passionate and collaborative team of experts in clinical research, pharmacovigilance, and quality consulting.
We are diverse in many ways, yet our values unite us. Our values are how we work, not words on a wall. If they sound like you, you will feel at home here.
We look forward to welcoming your application.
Leads study start-up and regulatory activities for assigned countries or projects, coordinating site initiation readiness, compliant documentation, agreements, timelines, and regulatory strategy.
Leads study start-up and regulatory activities to achieve site initiation readiness, delivering compliant documentation, agreements, and milestones while coordinating with internal teams, clients, and external stakeholders.
Leads study start-up and regulatory activities for assigned countries or projects, coordinating site readiness, compliant documentation, agreements, timelines, and regulatory strategy across internal and external stakeholders.
Coordinate patient admissions by answering and routing calls, completing behavioral health prescreenings, documenting interactions, scheduling appointments, and following up on outstanding issues.
Coordinates healthcare intake for new ABA clients, managing eligibility information, BCBA assignments, insurance authorizations, staffing, schedules, and communication to help services begin smoothly.
