Clinical Research Associate

Primary responsibilities include assisting clinical research team and administration including records management, documents and materials management and data input. Also, obtaining and transferring information in accordance with employer and/or sponsor standard operating procedures (SOP), good clinical practice, European Union directives and legislations and clinical research protocol.

Systematic nature, accuracy and correctness;

Ability to work independently;

Resistance to stress and good communication skills;

Desirably secondary or higher education in medicine or natural sciences;

Proficiency in using common Microsoft programs;

Experience in documents management;

Excellent knowledge of English language; spoken Russian language is an advantage;

Pleasant working environment and opportunity for professional development;

Professional trainings;

Competitive compensation;

In order to apply for the job, send your CV and cover letter to kati.rein@egeeninc.com