Project Manager

Contract, full-time
3+ years

What should be done?

  • Manage the progress of projects;
  • Interact with the team on the completeness of the received medical data;
  • Make decisions regarding the possibility and ways of implementing Sponsor's requirements, taking into account the pros and cons of possible implementations;
  • Control the quality of work of medical writers at the stage of creating synopsis, protocols, final reports on projects;
  • Participate in building processes within the company.

Expectations from the candidate

  • University Degree in Medicine, Biology or Pharmaceutical Sciences; 
  • 3+ yeras of work experience in international pharmaceutical companies or large CIOs;
  • Understanding of the pharmaceutical market and clinical research, drug development process and applicable regulatory requirements;
  • Fluency in English (written and spoken) is required;
  • Basic knowledge and understanding of statistics;
  • Excellent interpersonal, oral and written communication skills;
  • Customer-oriented approach to work.

What do we offer?

  • Join the most promising project in the field of medical data in the country and in the world - creating a world leader in Real-World Evidence with subsequent integration with genetic data;
  • Work schedule: 5/2;
  • Salary is discussed individually with a candidate;
  • Medical insurance after a 3-month trial period;
  • Comfortable office in the city center;
  • Opportunity for professional growth in a dynamically developing company.
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