Bilingual Clinical Research Associate (CRA) - Canada

				Overview:

Medpace is a full-service clinical contract research organization (CRO). We provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries. Our mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. We leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective. Headquartered in Cincinnati, Ohio, employing more than 5,000 people across 40+ countries.

Responsibilities:

* 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; and
* Review of patient charts and clinical research data.  

Qualifications:

* Bachelor's degree in science from an accredited university;
* At least 1 year as a Clinical Research Associate or Clinical Research Coordinator;
* Bilingual in English and French;
* Thorough knowledge of the methodology related to the conduct and monitoring of clinical trials per ICH E-6 guidelines and per Part-C, Division 5 of the Health Canada Food and Drug regulations;
* Excellent interpersonal, written and verbal communication skills in English and French;
* Strong attention to detail and organization skills;
* Highly motivated, independent, flexible;
* Ability to travel between 60-80%;
* Ability to prioritize workload to meet timelines across multiple studies; and
* Proficient in Microsoft Office.
			

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