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.
- 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.
Qualifications
- 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.
Required Skills
Two (2) years of related experience is required.