Clinical Project Manager

Clinical Project Manager

Clario

Budapest or Remote, Hungary

Are you seeking a purposeful and rewarding Project Management career opportunity?

We are a global leader in comprehensive endpoint technologies for Clinical Trials, our dedicated medical imaging, eCOA, Cardiac Safety and Respiratory operations are growing in Hungary and with big ambitions and a clear vision for the future, now is the time to join us as a Clinical Project Manager (f/m/x)!

What you'll be doing:

  • Lead the Planning and Setup, Monitoring, and Closeout phases of complex global studies across a variety of therapeutic areas;
  • Monitor study timelines and manage the financial components of each study including participating in monthly billing & forecasting where required;
  • Identify potential study risks and mitigations, and escalate as appropriate;
  • Managing change requests & communicating all clarifications/revisions to project team;
  • Apply problem solving strategies to address customer issues and maintain issue tracking documentation to monitor progress and ensure timely resolution to customer escalations;
  • Present study services at Investigator Meetings or site initiation meetings as needed, and/or attend client meetings with Business Development and/or Operational teams to present Company services;
  • Coordinating site management of data collection with internal and external teams;
  • Manage internal/external negotiations and promote collaboration to foster a positive team environment, effective communications, and efficient use of resources to meet study timelines and contractual obligations.

What we look for:

  • BSc, MSc, PhD in a relevant subject related to the Pharmaceutical/Healthcare/Life Science industry;
  • 1-3 years Clinical Research experience within a CRO or Pharmaceutical Research Organization and within in a project management related role;
  • Working knowledge of GCH, ICH guidelines and FDA regulations;
  • Experience in a client facing role with the ability to lead meetings with senior staff & global clientele;
  • Excellent knowledge of Clinical Research processes & practices;
  • Prior experience in Medical Imaging, eCOA, Cardiac Safety, Respiratory, IRT/RTSM, eConsent, ePRO or other eClinical/Clinical Technologies is also advantageous to applicants;
  • Experience using Planview or similar Project Management systems;
  • Excellent organizational, interpersonal, time management, and prioritization skills;
  • Excellent verbal and written communication skills, including ability to communicate effectively and confidently in English;
  • Working knowledge of Microsoft Office products;
  • Detail oriented and demonstrated responsiveness to inquiries and requests.

Apply Now

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