Monitor - Studii Medicale

Responsibilities:
- Locating and assessing the suitability of facilities at a study center;
- Briefing doctors/consultants (or investigators) on conducting the trial;
- Setting up the study centers, which includes ensuring each center has trial materials and checking that investigator knows exactly what has to be done;
- Monitoring the trial throughout its duration, which will involve visiting the study centers on a regular basis;
- Verifying that data entered on to the Case Report Forms is consistent with patient clinical notes known as source data/document verification (SDV);
- Collecting completed Case Report Forms 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 centers on completion of the trial; archiving study documentation and correspondence.

Cerinte
- Medical university degree or in natural sciences
- Experience in clinical trials is a plus
- 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 attentin 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
- Self-driven, independent character

Oferta (bonusuri, beneficii)
The motivational package is composed out of 4 parts:
A fix monthly income.
Substantial bonuses.
Hard and soft skills training.
Company mobile phone.