Epidemiologist III- Full time- Research, Design & Analysis

GENERAL SUMMARY:

• Under minimal direction from senior staff investigators, responsible for establishing goals, methods and procedures for large epidemiologic studies.
• Coordinates all aspects of design implementation.
• Conducts quality control analysis and monitors study progression.
• Identifies and addresses medical questions and issues.
• Prepares complex reports of analyses and publishes results in manuscripts.
• Writes all sections of grant applications.
• Meets regularly with the Principal Investigator to review project goals and progress, identify problems and possible solutions, and set priorities for activities of the entire multi-site project staff.
  * Responsible for managing the day-to-day functioning and clinical site operations.
  * Track and order supplies.
  * Work independently and under minimal supervision.
  * Coordinate and oversee daily operations of research studies.
  * Coordinate and assume responsibility for participant recruitment and follow-up, data collection, participant and project-status tracking, participant incentives, and reporting data to project leads.
  * Handle IRB submissions and develop regulatory study documents.
  * Work with grants managers to prepare legal contract agreements with collaborating institutions such as data use agreements (DUA), business associate agreements (BAA), , materials transfer agreements (MTA), and confidential disclosure agreements (CDA)