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À propos de ce poste Project Manager (f/m/x) Respiratory chez Clario

Clario · Sur site · Budapest

Join Clario, part of Thermo Fisher Scientific, as a Project Manager (f/m/d) in Budapest, Hungary, and play a critical role in bringing life-changing therapies to patients faster. In this position, you will lead clinical trial projects within our Respiratory business line, ensuring studies are delivered with high quality, on time, and within budget. Your work will help connect customers, study teams, and innovative clinical technologies to generate the evidence needed to advance healthcare worldwide.


What we offer

  • Competitive compensation
  • Attractive benefits focused on security, flexibility, support, and well-being
  • Engaging employee programs
  • Remote working within an international team
  • Home office allowance
  • OTP Szép Card
  • Flexible working hours

What you'll be doing

  • Lead the planning, setup, monitoring, and closeout phases of clinical trial projects
  • Act as the primary point of contact for clients, gathering requirements and translating them into actionable plans for internal teams
  • Coordinate project activities to ensure studies are delivered on time, within budget, and according to quality standards
  • Develop and maintain essential study documentation and project records
  • Oversee the distribution and tracking of study equipment and materials
  • Create and distribute project and study status reports to stakeholders
  • Manage study documentation and data archiving activities at project completion
  • Set clear expectations with customers and ensure commitments are met throughout the project lifecycle
  • Monitor study timelines, project milestones, and financial performance
  • Identify project risks, develop mitigation plans, and escalate issues when appropriate
  • Facilitate collaboration across internal teams, external partners, and customers to achieve study objectives
  • Lead communications, negotiations, and problem-solving efforts to resolve project challenges efficiently
  • Track customer issues and escalations, ensuring timely resolution and excellent customer service

What we look for

  • Bachelor’s degree or equivalent combination of education and relevant experience
  • Experience in project management, preferably within clinical research, pharmaceuticals, healthcare, life sciences, or a related industry
  • Understanding of clinical trials and the drug development process is advantageous
  • Knowledge of Good Clinical Practice (GCP) is a plus
  • Strong organizational, time management, and prioritization skills
  • Excellent interpersonal and stakeholder management abilities
  • Strong problem-solving skills with the ability to manage multiple priorities
  • Excellent verbal and written communication skills in English
  • Proficiency with standard business and project management software tools
  • Ability to work effectively in a dynamic, international, and customer-focused environment

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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À propos de Clario

Clario Privacy Policy Clario is a leading provider of endpoint data solutions to the clinical trials industry, generating high-quality clinical evidence for life sciences companies. We offer comprehensive evidence generation solutions that combine medical imaging, eCOA, precision motion, cardiac solutions and respiratory endpoints. For more than 50 years, Clario has delivered deep scientific expertise and broad endpoint technologies to help transform lives around the world. Our endpoint data solutions have supported over 30,000 clinical trials in more than 100 countries. Our global team of science, technology, and operational experts have supported over 70% of all FDA drug approvals since 20

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