Clinical Research Associate

- Medical university degree is mandatory
- Friendly and warm personality
- Competent in handling difficult situations
- Able to communicate effectively
- Able to remain calm and efficient under pressure
- Supportive of colleagues
- Charisma, natural radiance, and a well-groomed appearance
- Good knowledge of English is a must
- Strong multitasking abilities
- Exceptional attention to detail
- Proficiency in PC-based applications
- Availability to travel in the country and abroad
- Excellent planning and organizational skills and ability to work in a changing, multiple-demand setting in order to prioritize a large volume of work and meet deadlines efficiently and accurately.
- Ability to work independently.

Responsibilities:
- Locating and assessing the suitability of facilities at a study centre;
- Briefing doctors/consultants (or investigators) on conducting the trial;
- Setting up the study centres, which includes ensuring each centre has the trial materials and checking that the investigator knows exactly what has to be done;
- Monitoring the trial throughout its duration, which will involve visiting the study centres on a regular basis;
- Verifying that data entered on to the CRFs is consistent with patient clinical notes, known as source data/document verification (SDV);
- Collecting completed CRFs from hospitals and general practices;
- Writing visit reports;
- Filing and collating trial documentation and reports;
ensuring all unused trial supplies are accounted for;
- Closing down study centres on completion of the trial;
archiving study documentation and correspondence.
Only successful applicants will be contacted for an interview.

Clinical Trial Center is an independent full-service company in the area of clinical research with national coverage and providing phase II - IV clinical trial related services to pharmaceutical companies.