Research Area Specialist-Intermediate

Under limited supervision, responsible for the operation of clinical research studies with one or more faculty members or managers within a recognized unit. Assists with research project tasks to include recruitment, data collection, and the day to day operations of research projects. May act as liaison with other departments, divisions and organizations.

• 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.

Experience

• Plans, organizes and conducts one or more small or moderately complex clinical research projects according to plan; reviews progress and evaluates results.
• Serves as research study subject recruiter, interviewer, screener and evaluator of candidates for studies.
• 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.
• Prepares reports in response to inquiries from performance sites or regulatory organizations under supervision of the investigator.
• Maintains project documentation for study sites including contact lists, correspondence, reporting documentation, and compliance data according to standardized procedures.
• Performs all other duties as assigned.