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Clinical Project Manager, Specialty Solutions

Role overview

Qualifications

  • Bachelor’s degree or equivalent relevant experience; background in life sciences, pharmacy, nursing, healthcare or 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
  • Working knowledge of GCP, ICH guidelines, FDA regulations, SOPs and clinical trial quality requirements

Responsibilities

  • Lead clinical trial projects from study start-up through close-out, managing timelines, milestones, resources and project deliverables
  • 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

Key facts

Hard skills

Other skills

  • Quality Assurance
  • Communication
  • Leadership

About the company

Clario logo

Clario

  • Clinical Research (CRO)
  • XLarge
  • 1,001–5,000
Clario is a leading healthcare research and technology company that generates high quality clinical evidence for our pharmaceutical, biotech, and medical device partners. We offer comprehensive evidence generation solutions that combine eCOA, cardiac safety, medical imaging, precision motion, and respiratory endpoints. Since our founding more than 50 years ago, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported clinical trials over 26,000 times in more than 100 countries. Our global team of science, technology, and operational experts have supported over 60% of all FDA drug approvals since 2019. For more information, visit Clario.com

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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.

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