CLINICAL RESEARCH ASSOCIATE/PH Company/ONLU
2012-10-16
CLINICAL RESEARCH ASSOCIATE/PH Company/ONLU
Four our client, original PH Company based in Prague, we are looking for Clinical Research Associate with a minimum of 2 years monitoring experience. The responsibility of a Clinical Research Associate (CRA) is to perform the clinical monitoring aspect of designated projects in accordance with applicable SOP and regulations. Responsibilities include performing clinical on-site monitoring activities (drive patient recruitment, source data verification, drug accountability, data collection), collecting regulatory documentation (when required), performing qualification, initiation, monitoring and termination of investigational sites in accordance with ICH GCP guidelines.
Support the development of company relationships with opinion leaders and set up good working relationship with investigational site staff. Mentor and train junior clinical team members as appropriate. Perform quality visits with CRO CRA´s.
Successful candidates will hold a Degree in a scientific or healthcare discipline and will have monitoring experience and strong expertise in a CRO or pharmaceutical environment. This is an office based role with possibility to working from home 1 day per week. A strong written and verbal communication skill in Czech language including good command of English is a must.
We offer to work in fast expanding company, friendly atmosphere, total rewards package which includes competitive compensation, excellent benefits and career and development opportunities
In case of interest please send your CV to Lucie Ondruchová at ondruchova@hays.cz
