Responsible for planning, designing, monitoring, coordinating, analyzing and producing scientific content for clinical and regulatory documents. Manages and reviews medical writing of study protocols, statistical analysis and study reports. Demonstrated ability to organize and coordinate work within schedule constraints and handle emergent requirements in a timely manner. Demonstrated ability to monitor important and complex projects concurrently. Knowledge of Microsoft Word, Excel, PowerPoint, and Lotus Notes/other email software. Demonstrated ability to effectively communicate verbally and in writing, to include writing and preparing memorandums, letters, and other official correspondence.

Education:

Master's degree in related field is required.

Experience:

Two (2) years of related experience is required. Develops, designs, and executes large and complex research projects, reviews progress, analyses data and evaluates results. Formulates research methods and suggests options for improving quality; identifies potential problems and recommends and implements solutions. Consults with users to refine or adapt methodologies to fit research requirements; collaborates in development of new techniques and instruments. Organizes, maintains the laboratory, researches and recommends equipment and maintains documentation and storage of biomaterials. Co-authors/authors scientific publications; presents at meetings and conferences; participates in acquiring research funding including writing grant proposals. Manages and reviews medical writing of study protocols, statistical analysis and study reports. Performs all other duties as assigned.