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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