Medpace is a global, full-service Clinical Research Organization (CRO) specializing in a multitude of therapeutic areas. Our headquarters are located in Cincinnati, Ohio, USA and we are active in over 45 countries across the globe. We continue to steadily grow and are looking to add to our team!
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; • Review of patient charts and clinical research data; and • Assistance with feasibilities and other tasks upon business requirements.
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 and Ukrainian. Travel: Extensive
WHY MEDPACE? Join Medpace, a mid-size global CRO that is growing and offers limitless opportunities in career growth and where you will be rewarded for strong performance. At Medpace, you will find work that is both challenging and rewarding and you will be given the tools and training to succeed.
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.