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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