Remote Working Medical Writer

Working remotely, you will be working for a respected US based mid-size global CRO.

Headquartered in Cincinnati, Ohio, employing approximately 3,500 people across almost 40 countries. They are a full-service clinical contract research organization (CRO) and they provide Phase I-IV clinical development services to the biotechnology, pharmaceutical and medical device industries.

Their mission is to accelerate the global development of safe and effective medical therapeutics through its scientific and disciplined approach. They leverage local regulatory and therapeutic expertise across all major areas including oncology, cardiology, metabolic disease, endocrinology, central nervous system, anti-viral and anti-infective.

Your responsibilities will be:

• Write clinical study reports, protocols, and protocol amendments 
• Coordinate quality control reviews of documents and maintain audit trails of changes; and
• Project manage assignments across cross-functional.