(SEND)STANDARD FOR EXCHANGE OF NON-CLINICAL DATA
Determine and analyze the source of data
Interact with the Scientific Departments in order to create standard formatting for various data sources.
Interact with the Scientific Departments in order to implement the terminology required by the standard.
Interact with MIS Personnel in order to create tools to populate standard templates with the data generated by various sources.
Provide training and support as required to departments generating study data and to Report Production’s staff.
Experience with preclinical data collection, systems and practices.
In-depth understanding of preclinical data.
Exposure to industry data standards and terminologies (e.g., CDISC data standards).
Analytical and details oriented.
Excellent communication and collaboration skills; proven experience establishing positive relationships within the workplace.
Leadership, Focused and Organized.
Good communication and listening skills. Ability to work well both in a team, as well as individually.
Proficient in MS Office (Word, Excel, Outlook).
Starting Date: ASAP
Fields marked with an asterisk (*) are required.