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Open nowPosted 8 days ago

Clinical Project Manager, Specialty Solutions

clarioclinical64 open roles

Where
Budapest
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Your applicationOpen nowClinical Project Manager, Specialty Solutionsclarioclinical · Budapest

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The clock on this job

Early applications get read.

13.3% of postings close within 7 days. Measured by our own scanner across the market. clarioclinical postings stay open a median of 16 days.

Share of postings closed within
  1. 2.1%1 day
  2. 4.6%3 days
  3. 13.3%7 days
  4. 21.3%14 days
  5. 35.7%30 days
  6. 59.1%60 days
This job: posted 8 days ago

clarioclinical median: 16 days open

The posting

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.

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