Join Clario, part of Thermo Fisher Scientific, as a Clinical Project Manager, Specialty Solutions in Budapest, Hungary and go beyond traditional clinical project management. You’ll not only lead clinical trial projects from start-up through close-out, but also identify opportunities to improve how studies are delivered, strengthen processes and quality, and help create safer, more effective ways of working. By connecting sponsors, sites and cross-functional teams, you’ll turn complex study requirements into solutions that support reliable evidence and better outcomes.
What we offer
- Competitive compensation
- Attractive benefits focused on security, flexibility, support and well-being
- Engaging employee programs
- Remote working and home office allowance
- OTP Szép Card
What you'll be doing
- Lead clinical trial projects from study start-up through close-out, managing timelines, milestones, resources and project deliverables.
- Look beyond day-to-day project delivery to identify improvements that strengthen study processes, quality and safety.
- Partner with sponsors, sites and cross-functional teams to translate study requirements into practical project plans and solutions.
- Monitor project performance, anticipate risks and remove obstacles to support consistent, high-quality delivery.
- Manage project financials, including billing, forecasting, scope changes, revenue reporting and pass-through costs.
- Ensure project teams understand and follow protocols, SOPs and applicable quality requirements, working closely with Quality Assurance when deviations or clarifications arise.
- Lead, train and support project teams, creating clear expectations and encouraging collaboration and continuous improvement.
- Contribute your project and clinical expertise to client meetings, Investigator Meetings and Business Development activities as needed.
What we look for
- Bachelor’s degree or equivalent relevant experience; a background in life sciences, pharmacy, nursing, healthcare or a related field is an advantage.
- Previous project or management experience in the clinical development of investigational medicines.
- 1+ years of clinical trials experience within a CRO or pharmaceutical research organization, ideally in a project management-related role.
- Working knowledge of GCP, ICH guidelines, FDA regulations, SOPs and clinical trial quality requirements.