EastHORN Clinical Services in CEE Ltd is a clinical contract research organisation (CRO) serving global pharmaceutical and biotechnology companies in the development of new medicines. The company has operations throughout Central and Eastern Europe.

Our international clients value our enthusiastic and flexible approach to meeting their needs and we are growing rapidly. To support our further growth we are looking for a

Project Manager

Responsibilities include but are not limited to:

  • Managing the day-to-day activities necessary for the successful completion of a project within EastHORN and client timelines and budget
  • Serving as the Project Lead for key business development opportunities, including the preparation and delivery of client presentations
  • Responsible for establishing excellent working relationships with client project teams to ensure client satisfaction and operational excellence
  • Defining and managing project resource needs to ensure on-time and on-budget deliverables for assigned projects
  • Providing ongoing leadership and performance feedback to project team members
  • Managing the preparation of the study budget and site contract negotiations
  • Identifying, contacting and managing external vendors if required for a successful study conduct
  • Responsible for ensuring the successful design, implementation, tracking, and revisions of project plans
  • Acting as an expert in regulatory affairs and operations in related CEE countries
  • Managing all aspects of a clinical study and accountable for timelines, budgets, and quality
  • Supporting project team, assisting in study-specific training and providing regular feedback to line managers on staff performance
  • Ensuring the protection of study subjects and managing adverse events reporting and follow up


  • University/College degree (life science preferred) or certification in a related allied health profession (e.g. nursing certification, medical or laboratory technology)
  • Minimum 5 years of clinical research experience in a pharmaceutical company or CRO
  • Excellent knowledge of drug development process, ICH/GCP guidelines and ability to lead a clinical project team
  • Demonstrated ability to inspire effective teamwork and motivate staff within a matrix environment
  • Excellent written and oral communication skills
  • Fluent in written and verbal English

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