We are looking to recruit committed individuals to organize, manage and monitor phase I - IV oncology clinical trials.
The role provides the opportunity to develop monitoring skills with advanced responsibilities, critical and central to the conduct of the clinical project. The CRA oversees the progress of a Clinical Trial, ensuring that it is conducted, recorded and reported in accordance with the protocol, Standard Operating Procedures (SOPs), Good Clinical Practice (GCP) and the applicable Regulatory requirements.
Participation in the proper investigator/site selection, participation in the investigator grants negotiations, trial agreement preparation and investigator payment status tracking, ensuring adherence to the payment schedule, follow up of current developments in the field of clinical research, participation in the general and project-specific training.
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. 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
Delete