Our Client is a well-known company in the drug development sector with outstanding reputation for delivering clinical research services. Due to acquisition of new projects, they are looking for Clinical Research Associates at different levels – from CRA to Sr CRA to be based either in one of their offices in Russia or to work from home.
Responsibilities:
- Site monitoring including initiation of clinical sites, maintenance of study files, writing of clinical trial reports, conduct of pre-study and initiation visits, liaise with vendors and other duties
- Site and registry management as prescribed in the project plans
- Organising and making presentations at Investigator Meetings
- Participation in the development of protocols and CRFs
- Liaising with CPM to evaluate needs, resources and timelines
Requirements:
- Minimum 3 years of experience in monitoring clinical trials
- Excellent site monitoring and site management skills and understanding of SAEs
- Degree or equivalent in a life science discipline
- Fluency in Russian and English
To apply for this role, please send your CV in English, to joanna.wieliczko@pharmaprofessionals.eu