Clinical Project Manager, Specialty Solutions

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

About Clarioclinical

• At Clario, part of Thermo Fisher Scientific, our purpose is to transform lives by unlocking better evidence.
• It’s a cause that unites and inspires us.
• It’s why we come to work—and how we empower our people to make a positive impact every day.
• Whether you're advancing clinical science, building innovative technology, or supporting our global teams, your work helps bring life-changing therapies to patients faster.

Responsibilities

• 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.

Requirements

• Working knowledge of GCP, ICH guidelines, FDA regulations, SOPs and clinical trial quality requirements.
• A continuous-improvement mindset, with the ability to look beyond the immediate task, identify opportunities and turn them into practical improvements.
• Strong organizational and leadership skills, paired with clear, collaborative communication.
• Ability to travel up to 20% when required.

Preferred

• 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.
• Medical imaging experience is an advantage.
• Confidence using Microsoft Word and Excel; experience with Access and Project is beneficial.

Benefits

• 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