Clinical Project Manager, Specialty Solutions

Clario; United States; Remote; USD 28,000 - 40,000; Full time

Benefits offered by this job

Competitive compensation

Remote working

Home office allowance

OTP Szép Card

Engaging employee programs

Job summary

Clario, part of Thermo Fisher Scientific, seeks a Clinical Project Manager to lead clinical trial projects from start-up to close-out in Budapest, Hungary. You’ll drive improvements in study delivery, quality and safety while coordinating sponsors, sites and cross-functional teams.

Responsibilities include managing timelines, resources and budgets, ensuring regulatory and SOP compliance, and mentoring project teams. Some travel up to 20% is required and remote work options are available.

Qualifications

• Bachelor's degree in life sciences or related field.
• Experience leading clinical projects or trial management.
• GCP/ICH knowledge and FDA regulations.
• Strong communication and organizational skills.

Responsibilities

• Lead clinical trial projects from start-up through close-out, managing timelines, milestones, resources and deliverables.
• Identify process improvements to strengthen study quality and safety.
• Collaborate with sponsors, sites and cross-functional teams to translate study requirements into plans.
• Monitor performance, risks and obstacles to ensure high quality delivery.
• Manage project financials including billing, forecasting and pass-through costs.
• Ensure compliance with protocols, SOPs and quality requirements; coordinate with QA.
• Lead and train teams, fostering collaboration and continuous improvement.
• Contribute to client meetings and business development activities as needed.

Skills

Leadership

Communication

Organizational skills

Problem solving

Education

Bachelor's degree in life sciences or related field

Tools

MS Word

Excel

Access

MS Project

Job description

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.
• 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.
• Medical imaging experience is an advantage.
• Confidence using Microsoft Word and Excel; experience with Access and Project is beneficial.
• Ability to travel up to 20% when required.

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.