Medpace, a global Clinical Research Organization (CRO) with headquarters in Cincinnati. USA. and an office in Lyon. France, is seeking CRA candidates to join our team. This position offers the unique opportunity to have an exciting career in the research of drug and medical device development while making a difference in the lives of patients.
Post : Clinical Research Associate (CRA)
Job Description :
• Conduct qualification, initiation, monitoring, and closeout visits at research sites in compliance with the approved protocol
• Provide communication with the medical site staff including coordinators, clinical research physicians, and their site staff
• Verify adequate investigator qualifications, training, and resources, including facilities, laboratories, equipment, and site personnel
• Verify medical records and research source documentation against case report form data and inform the site stafrvf any entry errors
• Ensure good documentation practices and protocol compliance, manage protocol deviations appropriately per SOPs, GCP. and applicable regulatory requirements
• Review regulatory documents
• Review medical device and/or investigational product/ drug accountability and inventory
• Verify and review adverse events, serious adverse events, concomitant medications, and corresponding illnesses to confirm accurate data reporting in accordance with the protocol
• Assess the clinical research site's patient recruitment and retention success and offer suggestions for improvement
• Complete monitoring reports and follow-up letters, which include providing summaries of the significant findings, deviations, deficiencies, and recommended actions to secure compliance
Candidate Profile :
• Minimum Bachelor’s degree, preferably in the Life Sciences field
• Excellent organizational and prioritization skills
• Great attention to detail and excellent oral and written communication skills in English and French
• Ability to travel 60-80% (France mainly)
• Valid driver's license
Job Location : France-Lyon
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