Clinical Project Manager

з/п не указана

Вакансия в архиве

Работодатель, вероятно, уже нашел нужного кандидата и больше не принимает отклики на эту вакансию

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Требуемый опыт работы: 3–6 лет

Полная занятость, полный день

Clinical Project Manager is ultimately responsible for clinical trial adherence to time frames and budget limits set forth by the client, as well as for the clinical trials compliance with the quality standards and applicable regulations.

Project manager serves as the main communication point between the client and CRO team involved into the study. PM also controls the vendors responsible for providing services to the company within the scope of the project, and coordinates activities related to trial sites.

This position presumes full scope of PM responsibilities:

  • Project planning
  • Project team managing, distribution of responsibilities within project team
  • Organization and conduct of study meetings
  • Vendor’s identification and management
  • Coordination of study logistics
  • Creation of study-specific documentation, guidelines, plans
  • Checking reports for all types of visits carried out by CRAs
  • Reporting to and communication with Sponsor
  • Timely reporting on project status to management
  • Coordination of investigator’s and hospital payments as well as payments to third-parties
  • Following up on budget issues with the sponsor
  • Participation in audits/inspections
  • Budgeting various activities related to the study together with the Financial Department and Business Development Department


  • Minimum 3-5 year Project manager experience in a CRO
  • Life Science degree
  • Fluent English, written and spoken
  • Sound management skills
  • Proven ability to recruit, train and motivate personnel
  • Results-oriented


Москва, Мясницкая улица, 48
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Вакансия опубликована 15 августа 2019 в Москве

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