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Candidate should have degree in medicine, life sciences, or pharmacy, good communication and organizing skills, fluency in English, literacy in computers.
Job holder is expected to be careful, accurate as well as proactive, flexible and client oriented and to be able to work under pressure and to meet deadlines.
Preferred Experience as CRA or in a related field, including medical, clinical, pharmaceutical, laboratory, research, data analysis, data management and/or technical writing is considered an advantage.
Responsible for setting-up and monitoring clinical trials across various therapeutic areas according to contracted services and in compliance with current legislation, ICH GCP and appropriate company/Sponsor procedures and quality standards, answering to Sponsor’s requests, building strong relationships with the sites.
We offer excellent work environment, on going training and good career development. We offer an attractive salary (ranging between 10000 and 20000 Eur/year)
A privately owned Contract Research Organisation (CRO) offering clinical research services to pharmaceutical and biotechnology industries.
Angajatorul a ales ca denumirea companiei să nu fie făcută publică.
Numele companiei va fi dezvăluit doar celor ce vor fi contactați de către angajator.
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