Clinical Research Associate
As a CRA, you will have the opportunity to work with innovative therapeutic fields and with challenging studies ranging from phase I – III. We are looking for proactive, positive and self-motivated individuals to join our supportive and dynamic team. If you want to be a vibrant part of our growing team in Europe, please review this opening:
DESCRIPTION OF JOB DUTIES
Conduct pre-study, initiation, monitoring, and closeout visits for research sites according to Medpace/Sponsor SOPs and GCP;Maintain ongoing site correspondence and site files;Complete visit reports and maintaining study-related databases;Oversight and interaction with clinical research sites; andReview of patient charts and clinical research data.QUALIFICATIONS/REQUIREMENTS
University degree in health-related field;Previous experience as a CRA and /or other related clinical research environment;Proven track record of demonstrating experience in clinical patient management, protocol, CRF, preparing of ISF, documentation to be submitted to competent authorities;Computer literacy;Excellent verbal and written communication skills in English.Travel: EXTENSIVE
WHAT TO EXPECT NEXT
We look forward to receiving your application. A member of our recruitment team will review your qualifications. If interested, you will be contacted for an interview.
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