Clinical Project Manager


Munich, Germany


  • Primary contact for client, contractors and vendors;
  • Monitoring trial progress with timely reporting up to senior management;
  • Managing on-time execution and conduct of clinical trials, including key milestones, study budget, vendor selection, and resourcing needs;
  • Development of study plans; Anticipating issues and proactively preparing mitigation plans;
  • Developing project team resource requirements and fostering team building;
  • Monitoring project activities for conformity to the project scope and specifications, while adhering to PSI’s philosophy and corporate goals;
  • Establishing open communication lines within and between project team members;
  • Identifying and selecting investigators and clinical sites, negotiating site budgets;
  • Delivering project team training;
  • Site management supervision and issue resolution;
  • Participation and presentation at Investigator and bid defense meetings.


  • MD, PharmD, or University degree in life sciences;
  • At least 5 years of industry experience;
  • Direct project management experience, preferably in a fast-paced CRO, covering global trials;
  • Experience in managing complex phase I through III trials, from start-up through database lock;
  • Strong experience in vendor management;
  • Experience in oncology, inflammatory disease, and/or infectious disease projects;
  • Excellent command of German and English;
  • Knowledge of Clinical Research environment in Germany;
  • Team oriented with superior communication and interpersonal skills, including a positive and professional attitude to tasks and projects;
  • Strong organizational, leadership and planning skills;
  • Demonstrated ability to meet tight deadlines, multi-task, be flexible and thrive in a fast-paced work environment;
  • Ability to effectively manage and motivate a project team;
  • Experience with bid defenses and/or delivering presentations;
  • Proficiency in standard MS Office applications and MS Project.

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