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:
* Responsible for the distribution of safety reports to regulatory authorities;
* Create and maintain project-related trackers and status reports;
* Distribute and track safety-related notifications;
* Conduct quality control reviews of departmental documents;
* Perform other tasks as needed.
Qualifications:
* High school diploma required, ideally studying for a bachelor's degree in life science;
* Ideally some administrative experience in a business setting;
* Experience of being involved with any audits will be advantageous;
* Good organisational skills and attention to detail;
* Excellent written and oral communication skills;
* Computer literacy (Microsoft Office Package);
* Fluency in English
We kindly ask that you submit applications in English.
Share this job:
Share this Job