Manage the implementation of projects; oversees recruitment, enrollment and follow-up procedures; align effort across the center; support the management of data collection and analysis of projects; develop and maintain materials and tools for study management and provide timely reports to project leads; track metrics and ensure progress towards study milestones.
Manage the design, launch, and sustainment of tobacco treatment & implementation science trials by overseeing recruitment and enrollment; develop and maintain study management tools to facilitate project progress; provide supervision for study staff.
Manage study-related meetings; prepare all materials necessary to drive activities forward during these meetings and communicate next steps to all attendees after meetings; track all feedback and lead integration of feedback into projects.
Assist with preparation of regulatory documentation; support regulatory compliance by maintaining documentation; prepare data for reporting and analysis by contributing to data management.
Contribute to manuscript preparation and presentations.
Serve as a supervisor for study staff via individualized meetings; serve as staff point person for external communications related to research performance.
Perform additional duties as assigned. Position is contingent upon grant funding.

Bachelor of Science and 2 to 3 years of experience or equivalent combination of education and experience is required.
Impeccable organization, verbal, written, and interpersonal skills.
Demonstrate familiarity with word processing, spreadsheet, database, and statistical software, and web-based applications.
Working knowledge of REDCap and SPSS.

Clinical Research Coordinator

About this role