This is an exciting opportunity to work within a fast paced, busy environment for a leading global provider of outsourced development services to the pharmaceutical, biotechnology and medical device industries.  

You will be responsible for creating, implementing, and maintaining clinical trials. You will write protocols, case report forms, and consent forms. You will ensure good clinical practices are followed.

Desired Skills and Experience:

* Medical or Nursing degree;

* Experienced in working as a CRA 1-3 years;

* Fluent Russian and English required;

* Excellent communication skills (both written and oral) and the ability to build effective relationships with trial centre staff and colleagues;

* The ability to motivate others;

* Numeracy and an eye for detail;

* The ability to multi-task and think on your feet;

* Good organisational, IT and administrative skills - the job involves a lot of documentation and recording of information through computerised processes such as clinical trial management systems and electronic data capture.