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:
* Provide day to day project support to the clinical safety department;
* Database entry;
* Tracking, reviewing and filing of safety documentation;
* Compile and distribute safety notification letters; and
* Interact with internal and external team members on the status of reports.
Qualifications:
* A minimum of a High School diploma or equivalent;
* At least 1 year of administrative experience;
* Excellent organizational and prioritization skills are needed;
* Knowledge of Microsoft Office required; and
* Applicants should have great attention to detail and excellent oral and written communication skills.
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