We are lookingtorecruitcommittedindividualstowork in a busyclinicalresearchdepartmentprovidingessentialmonitoringsupport.
The role providestheopportunitytodevelopmonitoringskillswithadvancedresponsibilities, critical and central totheconductoftheclinicalproject.
The CRA overseestheprogressof a Clinical Trial, ensuringthatitisconducted, recorded and reported in accordancewiththeprotocol, Standard OperatingProcedures (SOPs), Good ClinicalPractice (GCP) and theapplicableRegulatoryrequirements
While projects vary, your typical responsibilities might include :
Performing site selection, initiation, monitoring and close-out visits, plus maintaining appropriate documentation
Supporting the development of a subject recruitment plan
Establishing regular lines of communication plus administering protocol and related study training to assigned sites
Evaluating the quality and integrity of site practices escalating quality issues as appropriate
Managing progress by tracking regulatory submissions, recruitment, case report form (CRF) completion, and data query resolution
You will need to be comfortable collaborating and communicating with a variety of colleagues and customers. Ideally, you will also have a good basic knowledge of applicable clinical research regulatory requirements.
A Bachelor's degree in a health care or other scientific discipline or educational equivalent
At least 2 year of experience as a CRA
Preferably with oncology experience.
Location : Bucharest
If you want to make an impact in the global research market, where we are working to make a real difference in patient health, we ask you to apply now and join our team .
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