Associate

• Assist project managers with day-to-day operations of commercial clinical studies
• Support document preparation, maintenance, and filing
• Coordinate and support meetings
• Perform data management activities, including data entry and review
• Write external correspondence, including emails, memos, minutes, and reports
• Format documents and create document templates
• Track study status, materials, system accesses, and study team trainings
• Create and format Case Report Forms, manuals of operations, and other study-related documentation
• Maintain the project website
• Communicate with internal and external project staff

Explore Project Associate at Rho. Review requirements and application details.